A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653296



Internal ID15389948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5878655..5913873hg38UCSC Ensembl
Innerchr11:5899885..5935103hg19UCSC Ensembl
Innerchr11:5856461..5891679hg18UCSC Ensembl
Innerchr11:5856461..5891679hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3835219
hg1935219
hg1835219
hg1735219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515489
Supporting Variants
Samples
Known GenesOR52E4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653296
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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