A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8179n54



Internal ID20141603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4079225..4205501hg38UCSC Ensembl
chr3:4120909..4247185hg19UCSC Ensembl
chr3:4095909..4222185hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38126277
hg19126277
hg18126277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589434, nsv589431, nsv589426
SamplesHGDP01319
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8179n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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