A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1322



Internal ID15197711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75178563..75209806hg38UCSC Ensembl
Outerchr16:75212461..75243704hg19UCSC Ensembl
Outerchr16:73769962..73801205hg18UCSC Ensembl
Outerchr16:73769962..73801205hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3831244
hg1931244
hg1831244
hg1731244
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7286
Supporting Variants
SamplesNA19240
Known GenesCTRB2
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)nssv1322
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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