A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7646n54



Internal ID22775541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62064410..62066551hg38UCSC Ensembl
chr20:60639466..60641607hg19UCSC Ensembl
chr20:60072861..60075002hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382142
hg192142
hg182142
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586466, nsv586456, nsv586458, nsv586462, nsv586461, nsv586463, nsv586460
Samples
Known GenesTAF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7646n54
Frequency
Sample Size17421
Observed Gain19
Observed Loss12
Observed Complex0
Frequencyn/a


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