A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698794



Internal ID15088760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58076034..58104394hg38UCSC Ensembl
Innerchr11:57843506..57871866hg19UCSC Ensembl
Innerchr11:57600082..57628442hg18UCSC Ensembl
Innerchr11:57600082..57628442hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3828361
hg1928361
hg1828361
hg1728361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523101
Supporting Variants
Samples
Known GenesOR9Q1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698794
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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