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dbVar

Database of genomic structural variation

nsv6092582

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: 102 SVs from 22 studies. See in: genome view

Submitted genomic53,364,858-53,364,858

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6092582	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	53,364,858	53,364,858
nsv6092582	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	53,398,770	53,398,770

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17633554	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17633554	Submitted genomic		NC_000016.10:g.533 64858_53364859ins7 5	GRCh38 (hg38)		NC_000016.10	Chr16	53,364,858	53,364,858
nssv17633554	Remapped	Perfect	NC_000016.9:g.5339 8770_53398771ins75	GRCh37.p13	First Pass	NC_000016.9	Chr16	53,398,770	53,398,770

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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