A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv982



Internal ID15198233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1879030..1919180hg38UCSC Ensembl
Outerchr11:1900260..1940410hg19UCSC Ensembl
Outerchr11:1856836..1896986hg18UCSC Ensembl
Outerchr11:1856836..1896986hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3840151
hg1940151
hg1840151
hg1740151
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7213
Supporting Variants
SamplesNA19240
Known GenesLSP1
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)nssv982
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