A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522635



Internal ID15449928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:137697075..137747499hg38UCSC Ensembl
Innerchr8:138709318..138759742hg19UCSC Ensembl
Innerchr8:138778500..138828924hg18UCSC Ensembl
Innerchr8:138778500..138828924hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3850425
hg1950425
hg1850425
hg1750425
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706033
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522635
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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