A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522477



Internal ID15449770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:97181661..97197780hg38UCSC Ensembl
Innerchr8:98193889..98210008hg19UCSC Ensembl
Innerchr8:98263065..98279184hg18UCSC Ensembl
Innerchr8:98263065..98279184hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3816120
hg1916120
hg1816120
hg1716120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705843
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522477
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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