A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564311



Internal ID16351720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35138507..35144413hg38UCSC Ensembl
Innerchr14:35607713..35613619hg19UCSC Ensembl
Innerchr14:34677464..34683370hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg385907
hg195907
hg185907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3628n54
Supporting Variantsnssv825709
Samples
Known GenesKIAA0391
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564311
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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