A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834756



Internal ID15782026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105167384..105177639hg38UCSC Ensembl
Innerchr14:105633721..105643976hg19UCSC Ensembl
Innerchr14:104704766..104715021hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3810256
hg1910256
hg1810256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566177
Supporting Variants
Samples
Known GenesJAG2, NUDT14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834756
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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