A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9015n54



Internal ID20142439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38663996..38665351hg38UCSC Ensembl
chr4:38665617..38666972hg19UCSC Ensembl
chr4:38342012..38343367hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381356
hg191356
hg181356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594007, nsv594008, nsv594003, nsv594005, nsv594006
Samples
Known GenesFLJ13197, KLF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9015n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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