A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9963



Internal ID15193371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:67890453..67917356hg38UCSC Ensembl
Outerchr16:67924356..67951259hg19UCSC Ensembl
Outerchr16:66481857..66508760hg18UCSC Ensembl
Outerchr16:66481857..66508760hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3826904
hg1926904
hg1826904
hg1726904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1844
Supporting Variants
SamplesNA18507
Known GenesPSKH1
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)nssv9963
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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