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dbVar

Database of genomic structural variation

nsv5885249

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:7,951

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: 382 SVs from 31 studies. See in: genome view

Submitted genomic73,628,695-73,636,645

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5885249	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	73,628,695	73,636,645
nsv5885249	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	72,848,530	72,856,480

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17469223	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17469223	Submitted genomic		NC_000023.11:g.736 28695_73636645del	GRCh38 (hg38)		NC_000023.11	ChrX	73,628,695	73,636,645
nssv17469223	Remapped	Perfect	NC_000023.10:g.728 48530_72856480del	GRCh37.p13	First Pass	NC_000023.10	ChrX	72,848,530	72,856,480

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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