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dbVar

Database of genomic structural variation

nsv5614532

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: 422 SVs from 23 studies. See in: genome view

Submitted genomic132,396,715-132,396,715

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5614532	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	132,396,715	132,396,715
nsv5614532	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	131,530,743	131,530,743

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17165692	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
nssv17165692	Submitted genomic		NC_000023.11:g.132 396715_132396716in s1067	GRCh38 (hg38)		NC_000023.11	ChrX	132,396,715	132,396,715
nssv17165692	Remapped	Perfect	NC_000023.10:g.131 530743_131530744in s1067	GRCh37.p13	First Pass	NC_000023.10	ChrX	131,530,743	131,530,743

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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