A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525190



Internal ID15452483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144180232..144190505hg38UCSC Ensembl
Innerchr3:143899074..143909347hg19UCSC Ensembl
Innerchr3:145381764..145392037hg18UCSC Ensembl
Innerchr3:145381772..145392045hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3810274
hg1910274
hg1810274
hg1710274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701269
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525190
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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