A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834679



Internal ID15781949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104864919..104865985hg38UCSC Ensembl
Innerchr14:105331256..105332322hg19UCSC Ensembl
Innerchr14:104402301..104403367hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381067
hg191067
hg181067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566118
Supporting Variants
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834679
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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