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dbVar

Database of genomic structural variation

nsv5630578

Organism: Homo sapiens

Study:nstd207 (Ebert 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):Ebert 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: 279 SVs from 56 studies. See in: genome view

Submitted genomic35,795,935-35,795,935

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5630578	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	35,795,935	35,795,935
nsv5630578	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	35,763,712	35,763,712

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17144164	insertion	HG02587	Sequencing	Sequence alignment	2,330

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17144164	Submitted genomic		NC_000006.12:g.357 95935_35795936ins1 2224	GRCh38 (hg38)		NC_000006.12	Chr6	35,795,935	35,795,935
nssv17144164	Remapped	Perfect	NC_000006.11:g.357 63712_35763713ins1 2224	GRCh37.p13	First Pass	NC_000006.11	Chr6	35,763,712	35,763,712

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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