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dbVar

Database of genomic structural variation

nsv5653774

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: 106 SVs from 34 studies. See in: genome view

Submitted genomic108,835,879-108,835,879

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5653774	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	108,835,879	108,835,879
nsv5653774	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	109,229,655	109,229,655

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17076757	insertion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17076757	Submitted genomic		NC_000012.12:g.108 835879_108835880in s67	GRCh38 (hg38)		NC_000012.12	Chr12	108,835,879	108,835,879
nssv17076757	Remapped	Perfect	NC_000012.11:g.109 229655_109229656in s67	GRCh37.p13	First Pass	NC_000012.11	Chr12	109,229,655	109,229,655

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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