A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626959



Internal ID15850491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75204640..75222945hg38UCSC Ensembl
Outerchr16:75238538..75256843hg19UCSC Ensembl
Outerchr16:73796039..73814344hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3818306
hg1918306
hg1818306
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513707
Supporting Variants
Samples1
Known GenesCTRB1, CTRB2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626959
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer