A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527690



Internal ID15454983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:86662144..86745351hg38UCSC Ensembl
Innerchr3:86711294..86794501hg19UCSC Ensembl
Innerchr3:86793984..86877191hg18UCSC Ensembl
Innerchr3:86793984..86877191hg17UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3883208
hg1983208
hg1883208
hg1783208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704166
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527690
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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