A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938077



Internal ID15885347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14777465..14884242hg38UCSC Ensembl
Innerchr20:14758111..14864888hg19UCSC Ensembl
Innerchr20:14706111..14812888hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38106778
hg19106778
hg18106778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585483
Supporting Variants
Samples
Known GenesMACROD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938077
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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