A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10091



Internal ID15196020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:55789828..55846370hg38UCSC Ensembl
Outerchr16:55823740..55880282hg19UCSC Ensembl
Outerchr16:54381241..54437783hg18UCSC Ensembl
Outerchr16:54381241..54437783hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3856543
hg1956543
hg1856543
hg1756543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7284
Supporting Variants
SamplesNA18956
Known GenesCES1, CES5A
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)nssv10091
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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