A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3236n54



Internal ID22771131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:69828390..69832892hg38UCSC Ensembl
chr13:70402522..70407024hg19UCSC Ensembl
chr13:69300523..69305025hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg384503
hg194503
hg184503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562216, nsv562215, nsv562218
Samples
Known GenesKLHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3236n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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