A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518012



Internal ID15445305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:79859756..79871164hg38UCSC Ensembl
Innerchr5:79155579..79166987hg19UCSC Ensembl
Innerchr5:79191335..79202743hg18UCSC Ensembl
Innerchr5:79191335..79202743hg17UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3811409
hg1911409
hg1811409
hg1711409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695424
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518012
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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