A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10099



Internal ID15196012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75172821..75218693hg38UCSC Ensembl
Outerchr16:75206719..75252591hg19UCSC Ensembl
Outerchr16:73764220..73810092hg18UCSC Ensembl
Outerchr16:73764220..73810092hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3845873
hg1945873
hg1845873
hg1745873
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7286
Supporting Variants
SamplesNA18956
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)nssv10099
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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