A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528576



Internal ID15455869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:54410566..54425868hg38UCSC Ensembl
Innerchr5:53706396..53721698hg19UCSC Ensembl
Innerchr5:53742153..53757455hg18UCSC Ensembl
Innerchr5:53742153..53757455hg17UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3815303
hg1915303
hg1815303
hg1715303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705195
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528576
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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