A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4446n54



Internal ID18996622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32159287..32569140hg38UCSC Ensembl
chr15:32451488..32861341hg19UCSC Ensembl
chr15:30238780..30648633hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38409854
hg19409854
hg18409854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568866, nsv568872, nsv568865
Samples
Known GenesCHRNA7, GOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4446n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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