A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525301



Internal ID15105908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3657746..3668847hg38UCSC Ensembl
Innerchr16:3707747..3718848hg19UCSC Ensembl
Innerchr16:3647748..3658849hg18UCSC Ensembl
Innerchr16:3647748..3658849hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3811102
hg1911102
hg1811102
hg1711102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701407
Samples
Known GenesDNASE1, TRAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525301
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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