A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094060



Internal ID21277864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18684989..19954068hg38UCSC Ensembl
Innerchr14:19461466..20422227hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381269080
hg19960762
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114111
Supporting Variants
Samplessample26
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3, POTEG, POTEM
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094060
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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