A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527097



Internal ID15454390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6289087..6300560hg38UCSC Ensembl
Innerchr5:6289200..6300673hg19UCSC Ensembl
Innerchr5:6342200..6353673hg18UCSC Ensembl
Innerchr5:6342200..6353673hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3811474
hg1911474
hg1811474
hg1711474
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703476
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527097
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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