esv3841221

Organism: Homo sapiens

Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:54
Validation:Not tested
Clinical Assertions: No
Region Size:48,296

Publication(s):1000 Genomes Consortium Phase 3 Integrated SV

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: 829 SVs from 77 studies. See in: genome view

Remapped(Score: Perfect):97,712,155-97,760,452

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3841221	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
esv3841221	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv19646093	deletion	HG00106	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,290
essv19646094	deletion	HG00121	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,326
essv19646095	deletion	HG00140	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,472
essv19646096	deletion	HG00154	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,446
essv19646097	deletion	HG00178	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,406
essv19646098	deletion	HG00179	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,095
essv19646099	deletion	HG00180	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,031
essv19646100	deletion	HG00186	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,391
essv19646101	deletion	HG00252	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,570
essv19646102	deletion	HG00275	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,155
essv19646103	deletion	HG00319	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,162
essv19646104	deletion	HG00321	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,384
essv19646105	deletion	HG00323	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,081
essv19646106	deletion	HG00325	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,403
essv19646107	deletion	HG00343	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,020
essv19646108	deletion	HG00344	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,886
essv19646109	deletion	HG00366	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,572
essv19646110	deletion	HG00638	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,281
essv19646111	deletion	HG01060	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,683
essv19646112	deletion	HG01064	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,863
essv19646113	deletion	HG01077	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,787
essv19646114	deletion	HG01111	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,414
essv19646115	deletion	HG01167	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,580
essv19646116	deletion	HG01190	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,469
essv19646117	deletion	HG01191	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,249
essv19646118	deletion	HG01405	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,814
essv19646119	deletion	HG01464	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,831
essv19646120	deletion	HG01495	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,329
essv19646121	deletion	HG01527	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,631
essv19646122	deletion	HG01618	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,073
essv19646123	deletion	HG01632	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,359
essv19646124	deletion	HG01767	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,623
essv19646125	deletion	HG02343	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,047
essv19646126	deletion	HG02491	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,369
essv19646127	deletion	HG02655	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,369
essv19646128	deletion	HG02774	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,674
essv19646129	deletion	HG03672	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,546
essv19646130	deletion	HG03756	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,417
essv19646131	deletion	HG03803	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,515
essv19646132	deletion	HG04018	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,180
essv19646133	deletion	NA07357	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,777
essv19646134	deletion	NA11830	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,943
essv19646135	deletion	NA12283	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,365
essv19646136	deletion	NA12340	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,534
essv19646137	deletion	NA12812	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,515
essv19646138	deletion	NA12890	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,371
essv19646139	deletion	NA19648	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,140
essv19646140	deletion	NA20504	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,407
essv19646141	deletion	NA20516	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,702
essv19646142	deletion	NA20753	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,496
essv19646143	deletion	NA20769	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,107
essv19646144	deletion	NA20773	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,348
essv19646145	deletion	NA20800	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,274
essv19646146	deletion	NA21107	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,587

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv19646093	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646094	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646095	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646096	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646097	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646098	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646099	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646100	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646101	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646102	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646103	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646104	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646105	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646106	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646107	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646108	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646109	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646110	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646111	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646112	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646113	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646114	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646115	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646116	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646117	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646118	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646119	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646120	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646121	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646122	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646123	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646124	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646125	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646126	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646127	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646128	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646129	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646130	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646131	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646132	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646133	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646134	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646135	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646136	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646137	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646138	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646139	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646140	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646141	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646142	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646143	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646144	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646145	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646146	Remapped	Perfect	NC_000005.10:g.(97 712155_97712157)_( 97760450_97760452) del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,712,156 (-1, +1)	97,760,451 (-1, +1)
essv19646093	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646094	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646095	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646096	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646097	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646098	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646099	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646100	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646101	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646102	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646103	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646104	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646105	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646106	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646107	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646108	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646109	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646110	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646111	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646112	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646113	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646114	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646115	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646116	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646117	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646118	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646119	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646120	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646121	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646122	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646123	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646124	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646125	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646126	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646127	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646128	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646129	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646130	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646131	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646132	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646133	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646134	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646135	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646136	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646137	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)
essv19646138	Submitted genomic		NC_000005.9:g.(970 47859_97047861)_(9 7096154_97096156)d el	GRCh37 (hg19)		NC_000005.9	Chr5	97,047,860 (-1, +1)	97,096,155 (-1, +1)

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dbVar

Database of genomic structural variation

esv3841221

Links to Other Resources

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.