A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518417



Internal ID15445710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:58056522..58067170hg38UCSC Ensembl
Innerchr4:58922688..58933336hg19UCSC Ensembl
Innerchr4:58617445..58628093hg18UCSC Ensembl
Innerchr4:58763616..58774264hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3810649
hg1910649
hg1810649
hg1710649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695852
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518417
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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