A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517528



Internal ID15098135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5302665..5309352hg38UCSC Ensembl
Innerchr16:5352666..5359353hg19UCSC Ensembl
Innerchr16:5292667..5299354hg18UCSC Ensembl
Innerchr16:5292667..5299354hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386688
hg196688
hg186688
hg176688
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677022, nssv672175, nssv665896, nssv652281, nssv656882
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517528
Frequency
Sample Size2026
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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