A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834731



Internal ID16128687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105125040..105167162hg38UCSC Ensembl
Innerchr14:105591377..105633499hg19UCSC Ensembl
Innerchr14:104662422..104704544hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3842123
hg1942123
hg1842123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566155
Supporting Variants
Samples
Known GenesJAG2, MIR6765
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834731
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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