A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8943



Internal ID15534921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:87134286..87179069hg38UCSC Ensembl
Outerchr11:86845328..86890111hg19UCSC Ensembl
Outerchr11:86522976..86567759hg18UCSC Ensembl
Outerchr11:86522976..86567759hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3844784
hg1944784
hg1844784
hg1744784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv420
Supporting Variants
SamplesNA12156
Known GenesTMEM135
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)nssv8943
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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