A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518166



Internal ID15445459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:84503605..84611836hg38UCSC Ensembl
Innerchr5:83799423..83907654hg19UCSC Ensembl
Innerchr5:83835179..83943410hg18UCSC Ensembl
Innerchr5:83835179..83943410hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38108232
hg19108232
hg18108232
hg17108232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695587
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518166
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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