A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1965



Internal ID15541248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:112733998..112758957hg38UCSC Ensembl
Outerchr11:112604721..112629680hg19UCSC Ensembl
Outerchr11:112109931..112134890hg18UCSC Ensembl
Outerchr11:112109931..112134890hg17UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3815063
hg1915063
hg1815063
hg1715063
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv496
Supporting Variants
SamplesNA18555
Known Genes
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)nssv1965
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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