A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518787



Internal ID15446080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:104714075..104763724hg38UCSC Ensembl
Innerchr4:105635232..105684881hg19UCSC Ensembl
Innerchr4:105854681..105904330hg18UCSC Ensembl
Innerchr4:105992836..106042485hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3849650
hg1949650
hg1849650
hg1749650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694274
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518787
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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