A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525322



Internal ID15105929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:74017114..74017477hg38UCSC Ensembl
Innerchr11:73728159..73728522hg19UCSC Ensembl
Innerchr11:73405807..73406170hg18UCSC Ensembl
Innerchr11:73405807..73406170hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38364
hg19364
hg18364
hg17364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701432
Samples
Known GenesC2CD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525322
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