A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4332n54



Internal ID20137756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23360531..23438636hg38UCSC Ensembl
chr15:23605678..23683783hg19UCSC Ensembl
chr15:21157119..21235224hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3878106
hg1978106
hg1878106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568301, nsv568308
Samples
Known GenesGOLGA8S
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4332n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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