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dbVar

Database of genomic structural variation

nsv5503168

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop 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:101

Publication(s):Byrska-Bishop 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: 53 SVs from 16 studies. See in: genome view

Submitted genomic16,758,051-16,758,151

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5503168	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	16,758,051	16,758,151
nsv5503168	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	16,779,598	16,779,698

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17042998	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17042998	Submitted genomic		NC_000011.10:g.167 58051_16758151dup	GRCh38 (hg38)		NC_000011.10	Chr11	16,758,051	16,758,151
nssv17042998	Remapped	Perfect	NC_000011.9:g.1677 9598_16779698dup	GRCh37.p13	First Pass	NC_000011.9	Chr11	16,779,598	16,779,698

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)
nssv17042998	<0.001	1	6404

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