A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4226



Internal ID15192267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75179186..75209750hg38UCSC Ensembl
Outerchr16:75213084..75243648hg19UCSC Ensembl
Outerchr16:73770585..73801149hg18UCSC Ensembl
Outerchr16:73770585..73801149hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3830565
hg1930565
hg1830565
hg1730565
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7286
Supporting Variants
SamplesNA12878
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)nssv4226
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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