A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566178



Internal ID16006901
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 StatusM
Merged Variantsdgv3982n54
Supporting Variantsnssv834757
Samples
Known GenesJAG2, NUDT14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566178
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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