A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526585



Internal ID15453878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35967566..35977275hg38UCSC Ensembl
Innerchr3:36009058..36018767hg19UCSC Ensembl
Innerchr3:35984062..35993771hg18UCSC Ensembl
Innerchr3:35984062..35993771hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg389710
hg199710
hg189710
hg179710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv280n21
Supporting Variantsnssv702903
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526585
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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