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dbVar

Database of genomic structural variation

nsv5916796

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

Submitted genomic114,526,438-114,526,507

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5916796	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	114,526,438	114,526,507
nsv5916796	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	114,397,160	114,397,229

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17368433	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17368433	Submitted genomic		NC_000011.10:g.114 526438_114526507de l	GRCh38 (hg38)		NC_000011.10	Chr11	114,526,438	114,526,507
nssv17368433	Remapped	Perfect	NC_000011.9:g.1143 97160_114397229del	GRCh37.p13	First Pass	NC_000011.9	Chr11	114,397,160	114,397,229

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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