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dbVar

Database of genomic structural variation

nsv5937920

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:912

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: 318 SVs from 37 studies. See in: genome view

Submitted genomic99,291,653-99,292,564

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5937920	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	99,291,653	99,292,564
nsv5937920	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	99,831,858	99,832,769

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17379484	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17379484	Submitted genomic		NC_000015.10:g.992 91653_99292564del	GRCh38 (hg38)		NC_000015.10	Chr15	99,291,653	99,292,564
nssv17379484	Remapped	Perfect	NC_000015.9:g.9983 1858_99832769del	GRCh37.p13	First Pass	NC_000015.9	Chr15	99,831,858	99,832,769

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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