A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938517



Internal ID16232473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:15354928..15380171hg38UCSC Ensembl
Innerchr20:15335574..15360816hg19UCSC Ensembl
Innerchr20:15283574..15308816hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3825244
hg1925243
hg1825243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585630
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)nssv938517
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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