esv3501985

Organism: Homo sapiens

Study:estd59 (1000 Genomes Consortium Pilot Project)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:34
Validation:Yes
Clinical Assertions: No
Region Size:15,801

Publication(s):1000 Genomes Project Consortium et al. 2010

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 123 SVs from 35 studies. See in: genome view

Remapped(Score: Perfect):41,453,908-41,469,728

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3501985	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
esv3501985	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
esv3501985	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv7722592	deletion	SAMN00001592	Sequencing	Split read mapping	12,716
essv7722593	deletion	SAMN00001693	Sequencing	Split read mapping	10,093
essv7722594	deletion	SAMN00001623	Sequencing	Split read mapping	10,870
essv7722595	deletion	SAMN00001660	Sequencing	Split read mapping	13,045
essv7722596	deletion	SAMN00001569	Sequencing	Split read mapping	9,598
essv7722597	deletion	SAMN00001530	Sequencing	Split read mapping	9,564
essv7722599	deletion	SAMN00001586	Sequencing	Split read mapping	8,856
essv7722600	deletion	SAMN00001603	Sequencing	Split read mapping	13,918
essv7722601	deletion	SAMN00001649	Sequencing	Split read mapping	13,082
essv7722602	deletion	SAMN00001624	Sequencing	Split read mapping	10,264
essv7722603	deletion	SAMN00801051	Sequencing	Split read mapping	14,990
essv7722604	deletion	SAMN00801317	Sequencing	Split read mapping	13,343
essv7722605	deletion	SAMN00001591	Sequencing	Split read mapping	13,341
essv7722606	deletion	SAMN00001616	Sequencing	Split read mapping	16,444
essv7722607	deletion	SAMN00001601	Sequencing	Split read mapping	14,986
essv7722608	deletion	SAMN00001671	Sequencing	Split read mapping	10,275
essv7722610	deletion	SAMN00001648	Sequencing	Split read mapping	15,747
essv7722611	deletion	SAMN00001663	Sequencing	Split read mapping	12,931
essv7722612	deletion	SAMN00001556	Sequencing	Split read mapping	17,127
essv7722613	deletion	SAMN00001644	Sequencing	Split read mapping	14,069
essv7722614	deletion	SAMN00797054	Sequencing	Split read mapping	11,153
essv7722615	deletion	SAMN00801031	Sequencing	Split read mapping	9,208
essv7722616	deletion	SAMN00001596	Sequencing	Split read mapping	14,505
essv7722617	deletion	SAMN00001585	Sequencing	Split read mapping	11,247
essv7722618	deletion	SAMN00001525	Sequencing	Split read mapping	19,957
essv7722619	deletion	SAMN00001613	Sequencing	Split read mapping	15,037
essv7722621	deletion	SAMN00001633	Sequencing	Split read mapping	13,751
essv7722622	deletion	SAMN00800266	Sequencing	Split read mapping	11,909
essv7722623	deletion	SAMN00001629	Sequencing	Split read mapping	12,063
essv7722624	deletion	SAMN00001637	Sequencing	Split read mapping	13,785
essv7722625	deletion	SAMN00801237	Sequencing	Split read mapping	9,493
essv7722626	deletion	SAMN00001580	Sequencing	Split read mapping	12,837
essv7722627	deletion	SAMN00001625	Sequencing	Split read mapping	10,737
essv7722628	deletion	SAMN00001606	Sequencing	Split read mapping	15,404

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv7722592	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722593	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722594	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722595	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722596	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722597	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722599	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722600	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722601	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722602	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722603	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722604	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722605	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722606	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722607	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722608	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722610	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722611	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722612	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722613	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722614	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722615	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722616	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722617	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722618	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722619	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722621	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722622	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722623	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722624	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722625	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722626	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722627	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722628	Remapped	Perfect	NC_000012.12:g.(41 453908_41453928)_( 41469709_41469728) del	GRCh38.p12	First Pass	NC_000012.12	Chr12	41,453,923 (-15, +5)	41,469,723 (-14, +5)
essv7722592	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722593	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722594	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722595	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722596	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722597	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722599	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722600	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722601	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722602	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722603	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722604	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722605	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722606	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722607	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722608	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722610	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722611	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722612	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722613	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722614	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722615	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722616	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722617	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722618	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722619	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722621	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722622	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722623	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722624	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722625	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722626	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722627	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722628	Remapped	Perfect	NC_000012.11:g.(41 847710_41847730)_( 41863511_41863530) del	GRCh37.p13	First Pass	NC_000012.11	Chr12	41,847,725 (-15, +5)	41,863,525 (-14, +5)
essv7722592	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722593	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722594	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722595	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722596	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722597	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722599	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722600	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722601	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722602	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722603	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722604	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722605	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722606	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722607	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722608	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722610	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722611	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722612	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722613	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722614	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722615	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722616	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722617	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722618	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722619	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722621	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722622	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722623	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722624	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722625	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)
essv7722626	Submitted genomic		NC_000012.10:g.(40 133977_40133997)_( 40149778_40149797) del	NCBI36 (hg18)		NC_000012.10	Chr12	40,133,992 (-15, +5)	40,149,792 (-14, +5)

Showing 100 of 102

Validation Information

Variant Call ID	Experiment ID	Sample ID	Method	Analysis	Result
essv7722618	36	SAMN00001525	Digital array	Other	Fail
essv7722618	38	SAMN00001525	Digital array	Other	Fail
essv7722597	36	SAMN00001530	Digital array	Other	Fail
essv7722597	38	SAMN00001530	Digital array	Other	Fail
essv7722612	36	SAMN00001556	Digital array	Other	Fail
essv7722612	38	SAMN00001556	Digital array	Other	Fail
essv7722596	36	SAMN00001569	Digital array	Other	Fail
essv7722596	38	SAMN00001569	Digital array	Other	Fail
essv7722626	36	SAMN00001580	Digital array	Other	Fail
essv7722626	38	SAMN00001580	Digital array	Other	Fail
essv7722617	36	SAMN00001585	Digital array	Other	Fail
essv7722617	38	SAMN00001585	Digital array	Other	Fail
essv7722599	36	SAMN00001586	Digital array	Other	Fail
essv7722599	38	SAMN00001586	Digital array	Other	Fail
essv7722605	36	SAMN00001591	Digital array	Other	Fail
essv7722605	38	SAMN00001591	Digital array	Other	Fail
essv7722592	36	SAMN00001592	Digital array	Other	Fail
essv7722592	38	SAMN00001592	Digital array	Other	Fail
essv7722616	36	SAMN00001596	Digital array	Other	Fail
essv7722616	38	SAMN00001596	Digital array	Other	Fail
essv7722607	36	SAMN00001601	Digital array	Other	Fail
essv7722607	38	SAMN00001601	Digital array	Other	Fail
essv7722600	36	SAMN00001603	Digital array	Other	Fail
essv7722600	38	SAMN00001603	Digital array	Other	Fail
essv7722628	36	SAMN00001606	Digital array	Other	Fail
essv7722628	38	SAMN00001606	Digital array	Other	Fail
essv7722619	36	SAMN00001613	Digital array	Other	Fail
essv7722619	38	SAMN00001613	Digital array	Other	Fail
essv7722606	36	SAMN00001616	Digital array	Other	Fail
essv7722606	38	SAMN00001616	Digital array	Other	Fail
essv7722594	36	SAMN00001623	Digital array	Other	Fail
essv7722594	38	SAMN00001623	Digital array	Other	Fail
essv7722602	36	SAMN00001624	Digital array	Other	Fail
essv7722602	38	SAMN00001624	Digital array	Other	Fail
essv7722627	36	SAMN00001625	Digital array	Other	Fail
essv7722627	38	SAMN00001625	Digital array	Other	Fail
essv7722623	36	SAMN00001629	Digital array	Other	Fail
essv7722623	38	SAMN00001629	Digital array	Other	Fail
essv7722621	36	SAMN00001633	Digital array	Other	Fail
essv7722621	38	SAMN00001633	Digital array	Other	Fail
essv7722624	36	SAMN00001637	Digital array	Other	Fail
essv7722624	38	SAMN00001637	Digital array	Other	Fail
essv7722613	36	SAMN00001644	Digital array	Other	Fail
essv7722613	38	SAMN00001644	Digital array	Other	Fail
essv7722610	36	SAMN00001648	Digital array	Other	Fail
essv7722610	38	SAMN00001648	Digital array	Other	Fail
essv7722601	36	SAMN00001649	Digital array	Other	Fail
essv7722601	38	SAMN00001649	Digital array	Other	Fail
essv7722595	36	SAMN00001660	Digital array	Other	Fail
essv7722595	38	SAMN00001660	Digital array	Other	Fail
essv7722611	36	SAMN00001663	Digital array	Other	Fail
essv7722611	38	SAMN00001663	Digital array	Other	Fail
essv7722608	36	SAMN00001671	Digital array	Other	Fail
essv7722608	38	SAMN00001671	Digital array	Other	Fail
essv7722593	36	SAMN00001693	Digital array	Other	Fail
essv7722593	38	SAMN00001693	Digital array	Other	Fail
essv7722614	36	SAMN00797054	Digital array	Other	Fail
essv7722614	38	SAMN00797054	Digital array	Other	Fail
essv7722622	36	SAMN00800266	Digital array	Other	Fail
essv7722622	38	SAMN00800266	Digital array	Other	Fail
essv7722615	36	SAMN00801031	Digital array	Other	Fail
essv7722615	38	SAMN00801031	Digital array	Other	Fail
essv7722603	36	SAMN00801051	Digital array	Other	Fail
essv7722603	38	SAMN00801051	Digital array	Other	Fail
essv7722625	36	SAMN00801237	Digital array	Other	Fail
essv7722625	38	SAMN00801237	Digital array	Other	Fail
essv7722604	36	SAMN00801317	Digital array	Other	Fail
essv7722604	38	SAMN00801317	Digital array	Other	Fail
essv7722618	37	SAMN00001525	Sequencing	de novo sequence assembly	Pass
essv7722597	37	SAMN00001530	Sequencing	de novo sequence assembly	Pass
essv7722612	37	SAMN00001556	Sequencing	de novo sequence assembly	Pass
essv7722596	37	SAMN00001569	Sequencing	de novo sequence assembly	Pass
essv7722626	37	SAMN00001580	Sequencing	de novo sequence assembly	Pass
essv7722617	37	SAMN00001585	Sequencing	de novo sequence assembly	Pass
essv7722599	37	SAMN00001586	Sequencing	de novo sequence assembly	Pass
essv7722605	37	SAMN00001591	Sequencing	de novo sequence assembly	Pass
essv7722592	37	SAMN00001592	Sequencing	de novo sequence assembly	Pass
essv7722616	37	SAMN00001596	Sequencing	de novo sequence assembly	Pass
essv7722607	37	SAMN00001601	Sequencing	de novo sequence assembly	Pass
essv7722600	37	SAMN00001603	Sequencing	de novo sequence assembly	Pass
essv7722628	37	SAMN00001606	Sequencing	de novo sequence assembly	Pass
essv7722619	37	SAMN00001613	Sequencing	de novo sequence assembly	Pass
essv7722606	37	SAMN00001616	Sequencing	de novo sequence assembly	Pass
essv7722594	37	SAMN00001623	Sequencing	de novo sequence assembly	Pass
essv7722602	37	SAMN00001624	Sequencing	de novo sequence assembly	Pass
essv7722627	37	SAMN00001625	Sequencing	de novo sequence assembly	Pass
essv7722623	37	SAMN00001629	Sequencing	de novo sequence assembly	Pass
essv7722621	37	SAMN00001633	Sequencing	de novo sequence assembly	Pass
essv7722624	37	SAMN00001637	Sequencing	de novo sequence assembly	Pass
essv7722613	37	SAMN00001644	Sequencing	de novo sequence assembly	Pass
essv7722610	37	SAMN00001648	Sequencing	de novo sequence assembly	Pass
essv7722601	37	SAMN00001649	Sequencing	de novo sequence assembly	Pass
essv7722595	37	SAMN00001660	Sequencing	de novo sequence assembly	Pass
essv7722611	37	SAMN00001663	Sequencing	de novo sequence assembly	Pass
essv7722608	37	SAMN00001671	Sequencing	de novo sequence assembly	Pass
essv7722593	37	SAMN00001693	Sequencing	de novo sequence assembly	Pass
essv7722614	37	SAMN00797054	Sequencing	de novo sequence assembly	Pass
essv7722622	37	SAMN00800266	Sequencing	de novo sequence assembly	Pass
essv7722615	37	SAMN00801031	Sequencing	de novo sequence assembly	Pass
essv7722603	37	SAMN00801051	Sequencing	de novo sequence assembly	Pass
essv7722625	37	SAMN00801237	Sequencing	de novo sequence assembly	Pass
essv7722604	37	SAMN00801317	Sequencing	de novo sequence assembly	Pass

dbVar

Database of genomic structural variation

esv3501985

Links to Other Resources

Genome View

Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

Validation Information

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant