A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679070



Internal ID15415722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134702275..134728149hg38UCSC Ensembl
Innerchr11:134572169..134598043hg19UCSC Ensembl
Innerchr11:134077379..134103253hg18UCSC Ensembl
Innerchr11:134077379..134103253hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3825875
hg1925875
hg1825875
hg1725875
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)nssv679070
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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