A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452478



Internal ID18621282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26729809..26912779hg38UCSC Ensembl
Innerchr14:27199015..27381985hg19UCSC Ensembl
Innerchr14:26268855..26451825hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38182971
hg19182971
hg18182971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428294
Supporting Variants
SamplesNA18916
Known GenesMIR4307
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)nssv452478
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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