A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5614



Internal ID15197142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75168804..75222522hg38UCSC Ensembl
Outerchr16:75202702..75256420hg19UCSC Ensembl
Outerchr16:73760203..73813921hg18UCSC Ensembl
Outerchr16:73760203..73813921hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3853719
hg1953719
hg1853719
hg1753719
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7286
Supporting Variants
SamplesNA19129
Known GenesCTRB1, CTRB2, ZFP1
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)nssv5614
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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