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dbVar

Database of genomic structural variation

nsv6911137

Organism: Homo sapiens

Study:nstd229 (Jun et al. 2023)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:139

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: 113 SVs from 33 studies. See in: genome view

Submitted genomic112,331,777-112,331,915

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6911137	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	112,331,777	112,331,915
nsv6911137	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	112,202,500	112,202,638

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18588869	duplication	Sequencing	Split read and paired-end mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18588869	Submitted genomic		NC_000011.10:g.112 331777_112331915du p	GRCh38 (hg38)		NC_000011.10	Chr11	112,331,777	112,331,915
nssv18588869	Remapped	Perfect	NC_000011.9:g.1122 02500_112202638dup	GRCh37.p13	First Pass	NC_000011.9	Chr11	112,202,500	112,202,638

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv18588869	0.238	51194	212010

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