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dbVar

Database of genomic structural variation

nsv5671598

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:58

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

Submitted genomic110,048,092-110,048,149

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5671598	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	110,048,092	110,048,149
nsv5671598	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	109,291,320	109,291,377

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17165245	deletion	HG03371	Sequencing	Sequence alignment	2,852

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17165245	Submitted genomic		NC_000023.11:g.110 048092_110048149de lA	GRCh38 (hg38)		NC_000023.11	ChrX	110,048,092	110,048,149
nssv17165245	Remapped	Perfect	NC_000023.10:g.109 291320_109291377de lA	GRCh37.p13	First Pass	NC_000023.10	ChrX	109,291,320	109,291,377

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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