A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv830097



Internal ID16124053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:82014971..82036839hg38UCSC Ensembl
Innerchr14:82481315..82503183hg19UCSC Ensembl
Innerchr14:81551068..81572936hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3821869
hg1921869
hg1821869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565302
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv830097
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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