A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518022



Internal ID15445315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:112758758..112773605hg38UCSC Ensembl
Innerchr4:113679914..113694761hg19UCSC Ensembl
Innerchr4:113899363..113914210hg18UCSC Ensembl
Innerchr4:114037518..114052365hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3814848
hg1914848
hg1814848
hg1714848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695432
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518022
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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