A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134762



Internal ID15641262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68891543..69044364hg38UCSC Ensembl
Innerchr9:71506459..71659280hg19UCSC Ensembl
Innerchr9:70696279..70849100hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38152822
hg19152822
hg18152822
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614549
Supporting Variants
Samples
Known GenesFXN, PIP5K1B, PRKACG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1134762
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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