A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518568



Internal ID15099175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:29840417..29861040hg38UCSC Ensembl
Innerchr16:29851738..29872361hg19UCSC Ensembl
Innerchr16:29759239..29779862hg18UCSC Ensembl
Innerchr16:29759239..29779862hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3820624
hg1920624
hg1820624
hg1720624
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696011
Samples
Known GenesCDIPT, MVP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518568
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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