A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565623



Internal ID16006346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94393116..94635006hg38UCSC Ensembl
Innerchr14:94859453..95101343hg19UCSC Ensembl
Innerchr14:93929206..94171096hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38241891
hg19241891
hg18241891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832701
Samples
Known GenesSERPINA11, SERPINA12, SERPINA3, SERPINA4, SERPINA5, SERPINA9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565623
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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