A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528586



Internal ID15109193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4951303..5021669hg38UCSC Ensembl
Innerchr16:5001304..5071670hg19UCSC Ensembl
Innerchr16:4941305..5011671hg18UCSC Ensembl
Innerchr16:4941305..5011671hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3870367
hg1970367
hg1870367
hg1770367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705211
Samples
Known GenesSEC14L5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528586
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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