A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938040



Internal ID16231996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14393927..14474851hg38UCSC Ensembl
Innerchr20:14374573..14455497hg19UCSC Ensembl
Innerchr20:14322573..14403497hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3880925
hg1980925
hg1880925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585441
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)nssv938040
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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