A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586559



Internal ID16373968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63195172..63248817hg38UCSC Ensembl
Innerchr20:61826524..61880169hg19UCSC Ensembl
Innerchr20:61296969..61350614hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3853646
hg1953646
hg1853646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv943742
Samples
Known GenesBIRC7, MIR3196, NKAIN4, YTHDF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586559
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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