A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585417



Internal ID16372826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:11290966..11326103hg38UCSC Ensembl
Innerchr20:11271614..11306751hg19UCSC Ensembl
Innerchr20:11219614..11254751hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3835138
hg1935138
hg1835138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151203
SamplesHGDP00926
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585417
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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