A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4432n54



Internal ID20137856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31325674..31329118hg38UCSC Ensembl
chr15:31617877..31621321hg19UCSC Ensembl
chr15:29405169..29408613hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg383445
hg193445
hg183445
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568792, nsv568795, nsv568786, nsv568790, nsv568785, nsv568796, nsv568780
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4432n54
Frequency
Sample Size17421
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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