A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8929n54



Internal ID19001105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3766386..3768639hg38UCSC Ensembl
chr4:3768113..3770366hg19UCSC Ensembl
chr4:3737911..3740164hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg382254
hg192254
hg182254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593471, nsv593472
Samples
Known GenesADRA2C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8929n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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