A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520129



Internal ID15447422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:97234696..97239410hg38UCSC Ensembl
Innerchr8:98246924..98251638hg19UCSC Ensembl
Innerchr8:98316100..98320814hg18UCSC Ensembl
Innerchr8:98316100..98320814hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg384715
hg194715
hg184715
hg174715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697239
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520129
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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