A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526656



Internal ID8420931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46505480..46812751hg38UCSC Ensembl
Innerchr16:46539392..46846663hg19UCSC Ensembl
Innerchr16:45096893..45404164hg18UCSC Ensembl
Innerchr16:45096893..45404164hg17UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg38307272
hg19307272
hg18307272
hg17307272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702984
Samples
Known GenesANKRD26P1, C16orf87, MYLK3, ORC6, SHCBP1, VPS35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526656
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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