A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519286



Internal ID15446579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:170370660..170374114hg38UCSC Ensembl
Innerchr3:170088448..170091902hg19UCSC Ensembl
Innerchr3:171571142..171574596hg18UCSC Ensembl
Innerchr3:171571150..171574604hg17UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg383455
hg193455
hg183455
hg173455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696767
Samples
Known GenesSKIL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519286
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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