A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6485



Internal ID15190693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:121441627..121475831hg38UCSC Ensembl
Outerchr11:121312336..121346540hg19UCSC Ensembl
Outerchr11:120817546..120851750hg18UCSC Ensembl
Outerchr11:120817546..120851750hg17UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3834205
hg1934205
hg1834205
hg1734205
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7225
Supporting Variants
SamplesNA12156
Known GenesSORL1
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)nssv6485
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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