A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8174n54



Internal ID20141598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4019253..4242079hg38UCSC Ensembl
chr3:4060937..4283763hg19UCSC Ensembl
chr3:4035937..4258763hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38222827
hg19222827
hg18222827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589425, nsv589420, nsv589409, nsv589408
SamplesHGDP00133, 1782681313_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8174n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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