A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521898



Internal ID15102505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:61452104..61506561hg38UCSC Ensembl
Innerchr8:62364663..62419120hg19UCSC Ensembl
Innerchr8:62527217..62581674hg18UCSC Ensembl
Innerchr8:62527217..62581674hg17UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3854458
hg1954458
hg1854458
hg1754458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694669
Samples
Known GenesASPH, CLVS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521898
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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