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dbVar

Database of genomic structural variation

nsv6206827

Organism: Homo sapiens

Study:nstd214 (Naslavsky et al. 2022)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:291

Publication(s):Naslavsky et al. 2022

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

Submitted genomic68,691,320-68,691,610

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6206827	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	68,691,320	68,691,610
nsv6206827	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	68,983,659	68,983,949

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17934958	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17934958	Submitted genomic		NC_000015.10:g.686 91320_68691610del	GRCh38 (hg38)		NC_000015.10	Chr15	68,691,320	68,691,610
nssv17934958	Remapped	Perfect	NC_000015.9:g.6898 3659_68983949del	GRCh37.p13	First Pass	NC_000015.9	Chr15	68,983,659	68,983,949

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)
nssv17934958	0.001	2	1790

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