A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095619



Internal ID21277002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18525480..19954068hg38UCSC Ensembl
Innerchr14:19301957..20422227hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381428589
hg191120271
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110410
Supporting Variants
Samplessample244
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, OR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3, POTEG, POTEM
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095619
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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