A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526343



Internal ID15453636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65515974..65550454hg38UCSC Ensembl
Innerchr3:65501649..65536129hg19UCSC Ensembl
Innerchr3:65476689..65511169hg18UCSC Ensembl
Innerchr3:65476689..65511169hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3834481
hg1934481
hg1834481
hg1734481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702635
Samples
Known GenesMAGI1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526343
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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