A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8152n54



Internal ID20141576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:245736..278518hg38UCSC Ensembl
chr3:287419..320201hg19UCSC Ensembl
chr3:262419..295201hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3832783
hg1932783
hg1832783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589289, nsv589290
Samples1780862576_A
Known GenesCHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8152n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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