A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7284



Internal ID15205592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:55724212..55846370hg38UCSC Ensembl
Outerchr16:55758124..55880282hg19UCSC Ensembl
Outerchr16:54315625..54437783hg18UCSC Ensembl
Outerchr16:54315625..54437783hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38122159
hg19122159
hg18122159
hg17122159
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9316, nssv6671, nssv10957, nssv10091, nssv10958
SamplesNA12156, NA18956, NA15510, NA18517
Known GenesCES1, CES1P1, CES1P2, 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)nsv7284
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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