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dbVar

Database of genomic structural variation

nsv6976064

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:600

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: 151 SVs from 23 studies. See in: genome view

Submitted genomic97,415,701-97,416,300

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6976064	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	97,415,701	97,416,300
nsv6976064	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	97,958,931	97,959,530

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18397890	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
nssv18397890	Submitted genomic		NC_000015.10:g.974 15701_97416300del	GRCh38 (hg38)		NC_000015.10	Chr15	97,415,701	97,416,300
nssv18397890	Remapped	Perfect	NC_000015.9:g.9795 8931_97959530del	GRCh37.p13	First Pass	NC_000015.9	Chr15	97,958,931	97,959,530

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)
nssv18397890	0.081	19960	251756

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