A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8655n54



Internal ID20142079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151814106..151833114hg38UCSC Ensembl
chr3:151531894..151550902hg19UCSC Ensembl
chr3:153014584..153033592hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3819009
hg1919009
hg1819009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592068, nsv592071
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8655n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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