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dbVar

Database of genomic structural variation

nsv5936400

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:10,202

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

Submitted genomic69,803,805-69,814,006

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5936400	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	69,803,805	69,814,006
nsv5936400	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	67,471,041	67,481,242

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17401031	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17401031	Submitted genomic		NC_000018.10:g.698 03805_69814006del	GRCh38 (hg38)		NC_000018.10	Chr18	69,803,805	69,814,006
nssv17401031	Remapped	Perfect	NC_000018.9:g.6747 1041_67481242del	GRCh37.p13	First Pass	NC_000018.9	Chr18	67,471,041	67,481,242

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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