A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525286



Internal ID15105893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12732928..12784735hg38UCSC Ensembl
Innerchr16:12826785..12878592hg19UCSC Ensembl
Innerchr16:12734286..12786093hg18UCSC Ensembl
Innerchr16:12734286..12786093hg17UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3851808
hg1951808
hg1851808
hg1751808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701391
Samples
Known GenesCPPED1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525286
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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