A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7644n54



Internal ID22775539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62064345..62066123hg38UCSC Ensembl
chr20:60639401..60641179hg19UCSC Ensembl
chr20:60072796..60074574hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381779
hg191779
hg181779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586452, nsv586453, nsv586455, nsv586465
Samples
Known GenesTAF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7644n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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