A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6671



Internal ID15190507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:55789714..55844494hg38UCSC Ensembl
Outerchr16:55823626..55878406hg19UCSC Ensembl
Outerchr16:54381127..54435907hg18UCSC Ensembl
Outerchr16:54381127..54435907hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3854781
hg1954781
hg1854781
hg1754781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7284
Supporting Variants
SamplesNA12156
Known GenesCES1
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)nssv6671
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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