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dbVar

Database of genomic structural variation

nsv6271941

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:69

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: 144 SVs from 37 studies. See in: genome view

Submitted genomic1,686,731-1,686,799

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6271941	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	1,686,731	1,686,799
nsv6271941	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	1,707,961	1,708,029

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17917710	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17917710	Submitted genomic		NC_000011.10:g.168 6731_1686799del	GRCh38 (hg38)		NC_000011.10	Chr11	1,686,731	1,686,799
nssv17917710	Remapped	Perfect	NC_000011.9:g.1707 961_1708029del	GRCh37.p13	First Pass	NC_000011.9	Chr11	1,707,961	1,708,029

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)
nssv17917710	0.009	17	1978

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