A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452135



Internal ID18274245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71888339..72093009hg38UCSC Ensembl
Innerchr11:71599385..71804055hg19UCSC Ensembl
Innerchr11:71277033..71481703hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38204671
hg19204671
hg18204671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428262
Supporting Variants
SamplesHGDP01089
Known GenesIL18BP, LOC100128494, LOC100133315, LRTOMT, MIR3165, NUMA1, RNF121
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)nssv452135
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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