A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452084



Internal ID18275194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55692211..55854408hg38UCSC Ensembl
Innerchr11:55459687..55621884hg19UCSC Ensembl
Innerchr11:55216263..55378460hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38162198
hg19162198
hg18162198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428256
Supporting Variants
SamplesNA19225
Known GenesOR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2
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)nssv452084
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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