A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10958



Internal ID15192860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:55808972..55831891hg38UCSC Ensembl
Outerchr16:55842884..55865803hg19UCSC Ensembl
Outerchr16:54400385..54423304hg18UCSC Ensembl
Outerchr16:54400385..54423304hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3822920
hg1922920
hg1822920
hg1722920
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7284
Supporting Variants
SamplesNA15510
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)nssv10958
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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