A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694502



Internal ID15084468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122878506..122882006hg38UCSC Ensembl
Innerchr11:122749214..122752714hg19UCSC Ensembl
Innerchr11:122254424..122257924hg18UCSC Ensembl
Innerchr11:122254424..122257924hg17UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg383501
hg193501
hg183501
hg173501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520988
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694502
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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