A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4468n54



Internal ID18996644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34414750..34690183hg38UCSC Ensembl
chr15:34706951..34982384hg19UCSC Ensembl
chr15:32494243..32769676hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38275434
hg19275434
hg18275434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569071, nsv568987, nsv569070, nsv569110, nsv569069, nsv569023, nsv569058, nsv569090
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2, MIR5588
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4468n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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