A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834757



Internal ID15782027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105167384..105178045hg38UCSC Ensembl
Innerchr14:105633721..105644382hg19UCSC Ensembl
Innerchr14:104704766..104715427hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3810662
hg1910662
hg1810662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566178
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)nssv834757
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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