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dbVar

Database of genomic structural variation

nsv5874011

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:114

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: 146 SVs from 28 studies. See in: genome view

Submitted genomic59,327,352-59,327,465

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5874011	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	59,327,352	59,327,465
nsv5874011	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	59,793,024	59,793,137

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17383428	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17383428	Submitted genomic		NC_000001.11:g.593 27352_59327465del	GRCh38 (hg38)		NC_000001.11	Chr1	59,327,352	59,327,465
nssv17383428	Remapped	Perfect	NC_000001.10:g.597 93024_59793137del	GRCh37.p13	First Pass	NC_000001.10	Chr1	59,793,024	59,793,137

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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