A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528718



Internal ID15456011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25086524..25375688hg38UCSC Ensembl
Innerchr5:25086633..25375797hg19UCSC Ensembl
Innerchr5:25122390..25411554hg18UCSC Ensembl
Innerchr5:25122390..25411554hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38289165
hg19289165
hg18289165
hg17289165
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705368
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528718
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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