A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702829



Internal ID15439481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134702275..134711509hg38UCSC Ensembl
Innerchr11:134572169..134581403hg19UCSC Ensembl
Innerchr11:134077379..134086613hg18UCSC Ensembl
Innerchr11:134077379..134086613hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg389235
hg199235
hg189235
hg179235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517742
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702829
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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