A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7664n54



Internal ID20141088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63154307..63248817hg38UCSC Ensembl
chr20:61785659..61880169hg19UCSC Ensembl
chr20:61256104..61350614hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3894511
hg1994511
hg1894511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586558, nsv586557
Samples1780854231_A, HGDP01079
Known GenesBIRC7, MIR124-3, MIR3196, NKAIN4, YTHDF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7664n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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