A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7205



Internal ID5090266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:79752623..79771405hg19UCSC Ensembl
Outerchr10:79422629..79441411hg18UCSC Ensembl
Outerchr10:79422629..79441411hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeOTHER Inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv951
SamplesNA19240
Known GenesPOLR3A
Method
AnalysisSample level sites were merged to generate a set of non-redundant variant regions. Two non-redundant inversion variants (chr 2 positions 89438708-89655419 and 89958869-91208466) were corrected from the original publication for coordinates and associated sample-level data.
PlatformCapillary
Comments
ReferenceKidd et al 2008
Pubmed ID18451855
Accession Number(s)nsv7205
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