A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834430



Internal ID15781700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104660017..104719329hg38UCSC Ensembl
Innerchr14:105126354..105185666hg19UCSC Ensembl
Innerchr14:104197399..104256711hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3859313
hg1959313
hg1859313
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566048
Supporting Variants
Samples
Known GenesINF2, MIR4710
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834430
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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