A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584805



Internal ID16372214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240213008..240253862hg38UCSC Ensembl
Innerchr2:241152425..241193279hg19UCSC Ensembl
Innerchr2:240801098..240841952hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3840855
hg1940855
hg1840855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151187
SamplesHGDP00806
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584805
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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