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dbVar

Database of genomic structural variation

nsv6177944

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:58

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: 81 SVs from 15 studies. See in: genome view

Submitted genomic8,586,962-8,587,019

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6177944	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	8,586,962	8,587,019
nsv6177944	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	8,628,925	8,628,982

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17917389	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17917389	Submitted genomic		NC_000010.11:g.858 6962_8587019del	GRCh38 (hg38)		NC_000010.11	Chr10	8,586,962	8,587,019
nssv17917389	Remapped	Perfect	NC_000010.10:g.862 8925_8628982del	GRCh37.p13	First Pass	NC_000010.10	Chr10	8,628,925	8,628,982

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)
nssv17917389	<0.001	1	1810

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