A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7687n54



Internal ID22775582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63830660..63836435hg38UCSC Ensembl
chr20:62462013..62467788hg19UCSC Ensembl
chr20:61932457..61938232hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385776
hg195776
hg185776
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586659, nsv586658, nsv586664, nsv586650, nsv586652, nsv586653, nsv586654
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7687n54
Frequency
Sample Size17421
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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