A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526916



Internal ID15107523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4057135..4143342hg38UCSC Ensembl
Innerchr3:4098819..4185026hg19UCSC Ensembl
Innerchr3:4073819..4160026hg18UCSC Ensembl
Innerchr3:4073819..4160026hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3886208
hg1986208
hg1886208
hg1786208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703277
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526916
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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