A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8265n54



Internal ID22776160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25988740..26144282hg38UCSC Ensembl
chr3:26030231..26185773hg19UCSC Ensembl
chr3:26005235..26160777hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38155543
hg19155543
hg18155543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589966, nsv589961, nsv589964, nsv589960, nsv589965, nsv589962, nsv589963, nsv589959
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8265n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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