A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11247



Internal ID15539332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1067274..1100709hg38UCSC Ensembl
Outerchr11:1067274..1094617hg19UCSC Ensembl
Outerchr11:1057274..1084617hg18UCSC Ensembl
Outerchr11:1057274..1084617hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3810080
hg1910080
hg1810080
hg1710080
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7638
Supporting Variants
SamplesNA15510
Known GenesMUC2
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)nssv11247
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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