A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518019



Internal ID15445312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15100292..15117355hg38UCSC Ensembl
Innerchr4:15101916..15118979hg19UCSC Ensembl
Innerchr4:14711014..14728077hg18UCSC Ensembl
Innerchr4:14778185..14795248hg17UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3817064
hg1917064
hg1817064
hg1717064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694060
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518019
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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