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dbVar

Database of genomic structural variation

nsv6887786

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:14,998

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: 175 SVs from 59 studies. See in: genome view

Submitted genomic97,266,010-97,281,007

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6887786	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	97,266,010	97,281,007
nsv6887786	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	99,025,767	99,040,764

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18341532	deletion	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
nssv18341532	Submitted genomic		NC_000010.11:g.972 66010_97281007del	GRCh38 (hg38)		NC_000010.11	Chr10	97,266,010	97,281,007
nssv18341532	Remapped	Perfect	NC_000010.10:g.990 25767_99040764del	GRCh37.p13	First Pass	NC_000010.10	Chr10	99,025,767	99,040,764

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)
nssv18341532	4e-06	1	270124

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