A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520215



Internal ID15447508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20429223..20443591hg38UCSC Ensembl
Innerchr5:20429332..20443700hg19UCSC Ensembl
Innerchr5:20465089..20479457hg18UCSC Ensembl
Innerchr5:20465089..20479457hg17UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3814369
hg1914369
hg1814369
hg1714369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697285
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520215
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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