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dbVar

Database of genomic structural variation

nsv5931598

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:218

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: 218 SVs from 33 studies. See in: genome view

Submitted genomic475,971-476,188

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5931598	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	475,971	476,188
nsv5931598	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	456,615	456,832

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17405114	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17405114	Submitted genomic		NC_000020.11:g.475 971_476188del	GRCh38 (hg38)		NC_000020.11	Chr20	475,971	476,188
nssv17405114	Remapped	Perfect	NC_000020.10:g.456 615_456832del	GRCh37.p13	First Pass	NC_000020.10	Chr20	456,615	456,832

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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