A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586563



Internal ID16373972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63221277..63293072hg38UCSC Ensembl
Innerchr20:61852629..61924424hg19UCSC Ensembl
Innerchr20:61323074..61394869hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3871796
hg1971796
hg1871796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150968
SamplesHGDP01048
Known GenesARFGAP1, BIRC7, FLJ16779, MIR3196, MIR4326, NKAIN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586563
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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