A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8653n54



Internal ID20142077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151792469..151836961hg38UCSC Ensembl
chr3:151510257..151554749hg19UCSC Ensembl
chr3:152992947..153037439hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3844493
hg1944493
hg1844493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592061, nsv592047, nsv592050
SamplesNINDS_268
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8653n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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