A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10957



Internal ID15192859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:55724212..55829996hg38UCSC Ensembl
Outerchr16:55758124..55863908hg19UCSC Ensembl
Outerchr16:54315625..54421409hg18UCSC Ensembl
Outerchr16:54315625..54421409hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38105785
hg19105785
hg18105785
hg17105785
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7284
Supporting Variants
SamplesNA15510
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)nssv10957
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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