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dbVar

Database of genomic structural variation

nsv5920773

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:29,476

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: 236 SVs from 45 studies. See in: genome view

Submitted genomic103,078,713-103,108,188

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5920773	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	103,078,713	103,108,188
nsv5920773	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	102,719,160	102,748,635

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17448932	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17448932	Submitted genomic		NC_000007.14:g.103 078713_103108188de l	GRCh38 (hg38)		NC_000007.14	Chr7	103,078,713	103,108,188
nssv17448932	Remapped	Perfect	NC_000007.13:g.102 719160_102748635de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	102,719,160	102,748,635

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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