A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583666



Internal ID16024389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:174324901..174346560hg38UCSC Ensembl
Innerchr2:175189629..175211288hg19UCSC Ensembl
Innerchr2:174897875..174919534hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3821660
hg1921660
hg1821660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv925609
Samples
Known GenesLOC285084, SP9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583666
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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