A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4459n54



Internal ID18996635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34380857..34567755hg38UCSC Ensembl
chr15:34673058..34859956hg19UCSC Ensembl
chr15:32460350..32647248hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38186899
hg19186899
hg18186899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568957, nsv568929, nsv568958, nsv568935, nsv568945, nsv568932, nsv568941, nsv568936, nsv568969, nsv568956, nsv568968
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4459n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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