A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4469n54



Internal ID18996645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34426393..34470157hg38UCSC Ensembl
chr15:34718594..34762358hg19UCSC Ensembl
chr15:32505886..32549650hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3843765
hg1943765
hg1843765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569011, nsv569017, nsv569044, nsv568991, nsv569025
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4469n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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