A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7640n54



Internal ID22775535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61252569..61253373hg38UCSC Ensembl
chr20:59827625..59828429hg19UCSC Ensembl
chr20:59261020..59261824hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38805
hg19805
hg18805
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586428, nsv586430, nsv586429
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7640n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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