A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv930156



Internal ID16224112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:193952787..194114434hg38UCSC Ensembl
Innerchr2:194817511..194979158hg19UCSC Ensembl
Innerchr2:194525756..194687403hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38161648
hg19161648
hg18161648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584085
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)nssv930156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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