A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685366



Internal ID15075332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33046843..33581367hg38UCSC Ensembl
Innerchr11:33068389..33602913hg19UCSC Ensembl
Innerchr11:33024965..33559489hg18UCSC Ensembl
Innerchr11:33024965..33559489hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38534525
hg19534525
hg18534525
hg17534525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521130
Supporting Variants
Samples
Known GenesCSTF3, CSTF3-AS1, HIPK3, KIAA1549L, LINC00294, TCP11L1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685366
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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