A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4470n54



Internal ID20137894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34426393..34483819hg38UCSC Ensembl
chr15:34718594..34776020hg19UCSC Ensembl
chr15:32505886..32563312hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3857427
hg1957427
hg1857427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569012, nsv569059, nsv569028, nsv569026, nsv568992, nsv569027, nsv569018, nsv569019
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4470n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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