A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585662



Internal ID16026385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:17610028..17630754hg38UCSC Ensembl
Innerchr20:17590673..17611399hg19UCSC Ensembl
Innerchr20:17538673..17559399hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3820727
hg1920727
hg1820727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152367
SamplesHGDP00515
Known GenesRRBP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585662
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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