A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4476n54



Internal ID18996652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34426604..34552372hg38UCSC Ensembl
chr15:34718805..34844573hg19UCSC Ensembl
chr15:32506097..32631865hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38125769
hg19125769
hg18125769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569101, nsv569066, nsv569100, nsv569108, nsv569065, nsv569009, nsv569099, nsv569114, nsv569109, nsv569067
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)dgv4476n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss53
Observed Complex0
Frequencyn/a


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