A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938031



Internal ID16231987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:12550696..12614724hg38UCSC Ensembl
Innerchr20:12531343..12595371hg19UCSC Ensembl
Innerchr20:12479343..12543371hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3864029
hg1964029
hg1864029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585430
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)nssv938031
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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