A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7641n54



Internal ID22775536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61693013..61729784hg38UCSC Ensembl
chr20:60268069..60304840hg19UCSC Ensembl
chr20:59701464..59738235hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3836772
hg1936772
hg1836772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586440, nsv586438, nsv586439
SamplesHGDP00033, HGDP00161, HGDP00208
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7641n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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