A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585704



Internal ID16373113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:20650266..20869392hg38UCSC Ensembl
Innerchr20:20630910..20850035hg19UCSC Ensembl
Innerchr20:20578910..20798035hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38219127
hg19219126
hg18219126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938807
Samples
Known GenesRALGAPA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585704
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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