A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586557



Internal ID16027280
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 StatusM
Merged Variantsdgv7664n54
Supporting Variantsnssv1150963
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)nsv586557
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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