A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150466



Internal ID15873251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:66977510..67012896hg38UCSC Ensembl
Innerchr2:67204642..67240028hg19UCSC Ensembl
Innerchr2:67058146..67093532hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3835387
hg1935387
hg1835387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582173
Supporting Variants
SamplesHGDP00151
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150466
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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