A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452439



Internal ID18621845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19751510..19947398hg38UCSC Ensembl
Innerchr14:20219669..20415557hg19UCSC Ensembl
Innerchr14:19289509..19485397hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38195889
hg19195889
hg18195889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428292
Supporting Variants
SamplesNA19189
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2
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)nssv452439
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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