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dbVar

Database of genomic structural variation

nsv6079265

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Wu et al. 2021

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: 110 SVs from 30 studies. See in: genome view

Submitted genomic43,352,186-43,352,186

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6079265	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	43,352,186	43,352,186
nsv6079265	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	43,319,924	43,319,924

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17571931	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17571931	Submitted genomic		NC_000006.12:g.433 52186_43352187ins6 6	GRCh38 (hg38)		NC_000006.12	Chr6	43,352,186	43,352,186
nssv17571931	Remapped	Perfect	NC_000006.11:g.433 19924_43319925ins6 6	GRCh37.p13	First Pass	NC_000006.11	Chr6	43,319,924	43,319,924

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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