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dbVar

Database of genomic structural variation

nsv5632241

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: 300 SVs from 36 studies. See in: genome view

Submitted genomic170,377,914-170,377,914

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5632241	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	170,377,914	170,377,914
nsv5632241	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	170,687,002	170,687,002

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17150921	insertion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17150921	Submitted genomic		NC_000006.12:g.170 377914_170377915in s1648	GRCh38 (hg38)		NC_000006.12	Chr6	170,377,914	170,377,914
nssv17150921	Remapped	Perfect	NC_000006.11:g.170 687002_170687003in s1648	GRCh37.p13	First Pass	NC_000006.11	Chr6	170,687,002	170,687,002

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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