A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505859



Internal ID20879132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47003677..47008752hg38UCSC Ensembl
chr16:47037588..47042663hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg385076
hg195076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182090
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505859
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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