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dbVar

Database of genomic structural variation

nsv5896876

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:90

Publication(s):Almarri et al. 2020

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: 113 SVs from 28 studies. See in: genome view

Submitted genomic22,027,675-22,027,764

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5896876	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	22,027,675	22,027,764
nsv5896876	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	22,027,904	22,027,993

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17439611	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17439611	Submitted genomic		NC_000006.12:g.220 27675_22027764dup	GRCh38 (hg38)		NC_000006.12	Chr6	22,027,675	22,027,764
nssv17439611	Remapped	Perfect	NC_000006.11:g.220 27904_22027993dup	GRCh37.p13	First Pass	NC_000006.11	Chr6	22,027,904	22,027,993

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)
nssv17439611	0.002	4	1606

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