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dbVar

Database of genomic structural variation

nsv5871709

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:2,379

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: 420 SVs from 25 studies. See in: genome view

Submitted genomic132,851,324-132,853,702

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5871709	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	132,851,324	132,853,702
nsv5871709	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	131,985,352	131,987,730

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17434468	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17434468	Submitted genomic		NC_000023.11:g.132 851324_132853702de l	GRCh38 (hg38)		NC_000023.11	ChrX	132,851,324	132,853,702
nssv17434468	Remapped	Perfect	NC_000023.10:g.131 985352_131987730de l	GRCh37.p13	First Pass	NC_000023.10	ChrX	131,985,352	131,987,730

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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