A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10884



Internal ID15192786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1905438..1967618hg38UCSC Ensembl
Outerchr11:1926668..1988848hg19UCSC Ensembl
Outerchr11:1883244..1945424hg18UCSC Ensembl
Outerchr11:1883244..1945424hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3862181
hg1962181
hg1862181
hg1762181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7213
Supporting Variants
SamplesNA15510
Known GenesMRPL23, TNNT3
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)nssv10884
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