A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv454448



Internal ID18619632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34784293..34954921hg38UCSC Ensembl
Innerchr4:34785915..34956543hg19UCSC Ensembl
Innerchr4:34462310..34632938hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38170629
hg19170629
hg18170629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428441
Supporting Variants
SamplesHGDP00449
Known Genes
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)nssv454448
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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