A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566261



Internal ID16006984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474495..105722674hg38UCSC Ensembl
Innerchr14:105940832..106189011hg19UCSC Ensembl
Innerchr14:105011877..105260056hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38248180
hg19248180
hg18248180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3998n54
Supporting Variantsnssv834925
Samples
Known GenesC14orf80, CRIP1, CRIP2, ELK2AP, MIR8071-1, MIR8071-2, TMEM121
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566261
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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