A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518407



Internal ID15445700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:4915784..4931098hg38UCSC Ensembl
Innerchr4:4917511..4932825hg19UCSC Ensembl
Innerchr4:4968412..4983726hg18UCSC Ensembl
Innerchr4:5035583..5050897hg17UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3815315
hg1915315
hg1815315
hg1715315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695838
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518407
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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