A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565667



Internal ID16353076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98703993..98731630hg38UCSC Ensembl
Innerchr14:99170330..99197967hg19UCSC Ensembl
Innerchr14:98240083..98267720hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3827638
hg1927638
hg1827638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3870n54
Supporting Variantsnssv832747
Samples
Known GenesC14orf177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565667
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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