A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7669n54



Internal ID22775564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63571331..63572021hg38UCSC Ensembl
chr20:62202684..62203374hg19UCSC Ensembl
chr20:61673128..61673818hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38691
hg19691
hg18691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586579, nsv586580, nsv586581
Samples
Known GenesHELZ2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7669n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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