A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9316



Internal ID15193581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:55735784..55826319hg38UCSC Ensembl
Outerchr16:55769696..55860231hg19UCSC Ensembl
Outerchr16:54327197..54417732hg18UCSC Ensembl
Outerchr16:54327197..54417732hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3890536
hg1990536
hg1890536
hg1790536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7284
Supporting Variants
SamplesNA18517
Known GenesCES1, CES1P1, CES1P2
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)nssv9316
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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