A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452434



Internal ID18621558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19379447..20088028hg38UCSC Ensembl
Innerchr14:19967167..20556187hg19UCSC Ensembl
Innerchr14:19037167..19626027hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38708582
hg19589021
hg18588861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428292
Supporting Variants
SamplesNA19113
Known GenesOR11H2, OR4K1, OR4K13, OR4K14, OR4K15, OR4K2, OR4K5, OR4L1, OR4M1, OR4N2, OR4Q3, POTEM
MethodBAC aCGH
AnalysisCopy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006).
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry_et_al_2008b
Pubmed ID18775914
Accession Number(s)nssv452434
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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