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dbVar

Database of genomic structural variation

nsv5667027

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:533

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: 367 SVs from 28 studies. See in: genome view

Submitted genomic71,523,282-71,523,814

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5667027	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	71,523,282	71,523,814
nsv5667027	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	70,743,132	70,743,664

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17167739	deletion	SAMN00007882	Sequencing	Sequence alignment	1,354

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17167739	Submitted genomic		NC_000023.11:g.715 23282_71523814delC	GRCh38 (hg38)		NC_000023.11	ChrX	71,523,282	71,523,814
nssv17167739	Remapped	Perfect	NC_000023.10:g.707 43132_70743664delC	GRCh37.p13	First Pass	NC_000023.10	ChrX	70,743,132	70,743,664

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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