A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564116



Internal ID16351525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27039536..27095650hg38UCSC Ensembl
Innerchr14:27508742..27564856hg19UCSC Ensembl
Innerchr14:26578582..26634696hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3856115
hg1956115
hg1856115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825059
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564116
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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