A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4433n54



Internal ID18996609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31325910..31328083hg38UCSC Ensembl
chr15:31618113..31620286hg19UCSC Ensembl
chr15:29405405..29407578hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382174
hg192174
hg182174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568782, nsv568783
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4433n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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