A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv352



Internal ID15201451
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
hg386474
hg196474
hg186474
hg176474
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5362, nssv2869
SamplesNA18555, NA19129
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)nsv352
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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