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dbVar

Database of genomic structural variation

nsv6103892

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: 92 SVs from 19 studies. See in: genome view

Submitted genomic32,491,586-32,491,586

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6103892	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	32,491,586	32,491,586
nsv6103892	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	32,887,573	32,887,573

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17641433	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17641433	Submitted genomic		NC_000022.11:g.324 91586_32491587ins6 2	GRCh38 (hg38)		NC_000022.11	Chr22	32,491,586	32,491,586
nssv17641433	Remapped	Perfect	NC_000022.10:g.328 87573_32887574ins6 2	GRCh37.p13	First Pass	NC_000022.10	Chr22	32,887,573	32,887,573

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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