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dbVar

Database of genomic structural variation

nsv5885421

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:93,825

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: 262 SVs from 42 studies. See in: genome view

Submitted genomic63,140,909-63,234,733

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5885421	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	63,140,909	63,234,733
nsv5885421	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	63,368,044	63,461,868

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17394112	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17394112	Submitted genomic		NC_000002.12:g.631 40909_63234733del	GRCh38 (hg38)		NC_000002.12	Chr2	63,140,909	63,234,733
nssv17394112	Remapped	Perfect	NC_000002.11:g.633 68044_63461868del	GRCh37.p13	First Pass	NC_000002.11	Chr2	63,368,044	63,461,868

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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