A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516064



Internal ID15096671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:67039649..67091161hg38UCSC Ensembl
Innerchr16:67073552..67125064hg19UCSC Ensembl
Innerchr16:65631053..65682565hg18UCSC Ensembl
Innerchr16:65631053..65682565hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3851513
hg1951513
hg1851513
hg1751513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683506, nssv673651, nssv665949, nssv660991
Samples
Known GenesCBFB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516064
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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