A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452088



Internal ID18274029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61049513..61191814hg38UCSC Ensembl
Innerchr11:60816985..60959286hg19UCSC Ensembl
Innerchr11:60573561..60715862hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38142302
hg19142302
hg18142302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428259
Supporting Variants
SamplesHGDP01086
Known GenesCD5, VPS37C
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)nssv452088
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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