A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7716n54



Internal ID22775611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64117405..64119126hg38UCSC Ensembl
chr20:62748758..62750479hg19UCSC Ensembl
chr20:62219202..62220923hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381722
hg191722
hg181722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586814, nsv586816, nsv586812, nsv586811, nsv586813
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7716n54
Frequency
Sample Size17421
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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