A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694223



Internal ID15084189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3078887..3080173hg38UCSC Ensembl
Innerchr3:3120571..3121857hg19UCSC Ensembl
Innerchr3:3095571..3096857hg18UCSC Ensembl
Innerchr3:3095571..3096857hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg381287
hg191287
hg181287
hg171287
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518298
Supporting Variants
Samples
Known GenesIL5RA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694223
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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