A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5362



Internal ID15196439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:63555836..63589650hg38UCSC Ensembl
Outerchr11:63323308..63357122hg19UCSC Ensembl
Outerchr11:63079884..63113698hg18UCSC Ensembl
Outerchr11:63079884..63113698hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg385466
hg195466
hg185466
hg175466
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv352
Supporting Variants
SamplesNA19129
Known GenesHRASLS2, PLA2G16
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv5362
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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