A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452206



Internal ID18273677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98936705..99229707hg38UCSC Ensembl
Innerchr11:98807435..99100438hg19UCSC Ensembl
Innerchr11:98312645..98605648hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38293003
hg19293004
hg18293004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428265
Supporting Variants
SamplesHGDP00474
Known GenesCNTN5
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)nssv452206
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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