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dbVar

Database of genomic structural variation

nsv5917639

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:106

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

Submitted genomic132,754,882-132,754,987

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5917639	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	132,754,882	132,754,987
nsv5917639	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	134,568,386	134,568,491

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17361044	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17361044	Submitted genomic		NC_000010.11:g.132 754882_132754987de l	GRCh38 (hg38)		NC_000010.11	Chr10	132,754,882	132,754,987
nssv17361044	Remapped	Perfect	NC_000010.10:g.134 568386_134568491de l	GRCh37.p13	First Pass	NC_000010.10	Chr10	134,568,386	134,568,491

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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