A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3261n54



Internal ID22771156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76885347..76886566hg38UCSC Ensembl
chr13:77459482..77460701hg19UCSC Ensembl
chr13:76357483..76358702hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg381220
hg191220
hg181220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562370, nsv562369, nsv562372
Samples
Known GenesKCTD12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3261n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer