A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452189



Internal ID18620485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:91051766..91186887hg38UCSC Ensembl
Innerchr11:90784934..90920055hg19UCSC Ensembl
Innerchr11:90424582..90559703hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38135122
hg19135122
hg18135122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428264
Supporting Variants
SamplesHGDP00478
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)nssv452189
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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