A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4429n54



Internal ID18996605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31325585..31327742hg38UCSC Ensembl
chr15:31617788..31619945hg19UCSC Ensembl
chr15:29405080..29407237hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382158
hg192158
hg182158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568787, nsv568775
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4429n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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