A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523933



Internal ID15451226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6152116..6183086hg38UCSC Ensembl
Innerchr11:6173346..6204316hg19UCSC Ensembl
Innerchr11:6129922..6160892hg18UCSC Ensembl
Innerchr11:6129922..6160892hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3830971
hg1930971
hg1830971
hg1730971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699779
Samples
Known GenesOR52B2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523933
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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