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dbVar

Database of genomic structural variation

nsv5536737

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

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: 157 SVs from 20 studies. See in: genome view

Submitted genomic94,695,714-94,695,714

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5536737	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	94,695,714	94,695,714
nsv5536737	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	95,707,942	95,707,942

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17013239	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17013239	Submitted genomic		NC_000008.11:g.946 95714_94695715ins6 4	GRCh38 (hg38)		NC_000008.11	Chr8	94,695,714	94,695,714
nssv17013239	Remapped	Perfect	NC_000008.10:g.957 07942_95707943ins6 4	GRCh37.p13	First Pass	NC_000008.10	Chr8	95,707,942	95,707,942

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)
nssv17013239	0.041	265	6404

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