A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv928232



Internal ID16222188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:185886008..185986497hg38UCSC Ensembl
Innerchr2:186750735..186851224hg19UCSC Ensembl
Innerchr2:186458980..186559469hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38100490
hg19100490
hg18100490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584023
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv928232
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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