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dbVar

Database of genomic structural variation

nsv5890529

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:70

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: 139 SVs from 22 studies. See in: genome view

Submitted genomic117,705,082-117,705,151

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5890529	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	117,705,082	117,705,151
nsv5890529	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	118,026,245	118,026,314

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17417743	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17417743	Submitted genomic		NC_000006.12:g.117 705082_117705151de l	GRCh38 (hg38)		NC_000006.12	Chr6	117,705,082	117,705,151
nssv17417743	Remapped	Perfect	NC_000006.11:g.118 026245_118026314de l	GRCh37.p13	First Pass	NC_000006.11	Chr6	118,026,245	118,026,314

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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