A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528639



Internal ID15109246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184228486..184262628hg38UCSC Ensembl
Innerchr3:183946274..183980416hg19UCSC Ensembl
Innerchr3:185428968..185463110hg18UCSC Ensembl
Innerchr3:185428976..185463118hg17UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3834143
hg1934143
hg1834143
hg1734143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705270
Samples
Known GenesALG3, CAMK2N2, ECE2, MIR1224, VWA5B2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528639
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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