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dbVar

Database of genomic structural variation

nsv5884615

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:107

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: 959 SVs from 29 studies. See in: genome view

Submitted genomic1,200,534-1,200,640

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5884615	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	1,200,534	1,200,640
nsv5884615	Remapped	Good	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	1,319,418	1,319,526

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17439197	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17439197	Submitted genomic		NC_000023.11:g.120 0534_1200640del	GRCh38 (hg38)		NC_000023.11	ChrX	1,200,534	1,200,640
nssv17439197	Remapped	Good	NC_000023.10:g.131 9418_1319526del	GRCh37.p13	First Pass	NC_000023.10	ChrX	1,319,418	1,319,526

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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