A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526375



Internal ID15453668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152044253..152058656hg38UCSC Ensembl
Innerchr5:151423814..151438217hg19UCSC Ensembl
Innerchr5:151404007..151418410hg18UCSC Ensembl
Innerchr5:151404007..151418410hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3814404
hg1914404
hg1814404
hg1714404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702671
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526375
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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