A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528626



Internal ID15455919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25819216..25847868hg38UCSC Ensembl
Innerchr5:25819325..25847977hg19UCSC Ensembl
Innerchr5:25855082..25883734hg18UCSC Ensembl
Innerchr5:25855082..25883734hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3828653
hg1928653
hg1828653
hg1728653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705256
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528626
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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