A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv821325



Internal ID16115281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18568381..19061863hg38UCSC Ensembl
Innerchr14:19344858..19649523hg19UCSC Ensembl
Innerchr14:18414858..18719523hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38493483
hg19304666
hg18304666
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563610
Supporting Variants
Samples
Known GenesLOC642426, OR11H12, POTEG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv821325
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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