A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151237



Internal ID15526202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14897008..15062977hg38UCSC Ensembl
Innerchr20:14877654..15043623hg19UCSC Ensembl
Innerchr20:14825654..14991623hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38165970
hg19165970
hg18165970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585548
Supporting Variants
SamplesHGDP00066
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151237
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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