A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151212



Internal ID15527134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14777465..15036594hg38UCSC Ensembl
Innerchr20:14758111..15017240hg19UCSC Ensembl
Innerchr20:14706111..14965240hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38259130
hg19259130
hg18259130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585484
Supporting Variants
SamplesHGDP00372
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151212
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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