A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4431n54



Internal ID18996607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31325674..31328232hg38UCSC Ensembl
chr15:31617877..31620435hg19UCSC Ensembl
chr15:29405169..29407727hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382559
hg192559
hg182559
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568784, nsv568779, nsv568778, nsv568788, nsv568789, nsv568793
Samples
Known GenesKLF13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4431n54
Frequency
Sample Size17421
Observed Gain20
Observed Loss11
Observed Complex0
Frequencyn/a


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