A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150963



Internal ID15531321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63154307..63236102hg38UCSC Ensembl
Innerchr20:61785659..61867454hg19UCSC Ensembl
Innerchr20:61256104..61337899hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3881796
hg1981796
hg1881796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586557
Supporting Variants
SamplesHGDP01079
Known GenesBIRC7, MIR124-3, YTHDF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150963
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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