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dbVar

Database of genomic structural variation

nsv5883212

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:83

Publication(s):Almarri et al. 2020

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: 408 SVs from 27 studies. See in: genome view

Submitted genomic82,370,867-82,370,949

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5883212	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	82,370,867	82,370,949
nsv5883212	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	81,626,316	81,626,398

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17469633	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17469633	Submitted genomic		NC_000023.11:g.823 70867_82370949del	GRCh38 (hg38)		NC_000023.11	ChrX	82,370,867	82,370,949
nssv17469633	Remapped	Perfect	NC_000023.10:g.816 26316_81626398del	GRCh37.p13	First Pass	NC_000023.10	ChrX	81,626,316	81,626,398

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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