A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938067



Internal ID15885337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14749245..15119638hg38UCSC Ensembl
Innerchr20:14729891..15100284hg19UCSC Ensembl
Innerchr20:14677891..15048284hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38370394
hg19370394
hg18370394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585469
Supporting Variants
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938067
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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