A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9938



Internal ID15540026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1090245..1105794hg38UCSC Ensembl
Outerchr11:1088181..1099702hg19UCSC Ensembl
Outerchr11:1078181..1089702hg18UCSC Ensembl
Outerchr11:1078181..1089702hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388716
hg198716
hg188716
hg178716
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7638
Supporting Variants
SamplesNA18507
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)nssv9938
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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