A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8933n54



Internal ID22776828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6254762..6301627hg38UCSC Ensembl
chr4:6256489..6303354hg19UCSC Ensembl
chr4:6307390..6354255hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3846866
hg1946866
hg1846866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593496, nsv593497
SamplesHGDP00817, HGDP01190
Known GenesWFS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8933n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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