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dbVar

Database of genomic structural variation

nsv5915084

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:981

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: 109 SVs from 25 studies. See in: genome view

Submitted genomic111,692,162-111,693,142

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5915084	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	111,692,162	111,693,142
nsv5915084	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	111,562,886	111,563,866

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17366040	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17366040	Submitted genomic		NC_000011.10:g.111 692162_111693142de l	GRCh38 (hg38)		NC_000011.10	Chr11	111,692,162	111,693,142
nssv17366040	Remapped	Perfect	NC_000011.9:g.1115 62886_111563866del	GRCh37.p13	First Pass	NC_000011.9	Chr11	111,562,886	111,563,866

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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