A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584672



Internal ID16372081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:230425261..230484173hg38UCSC Ensembl
Innerchr2:231289976..231348888hg19UCSC Ensembl
Innerchr2:230998220..231057132hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3858913
hg1958913
hg1858913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv933612
Samples
Known GenesSP100
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584672
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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