A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499561



Internal ID20872782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65946992..66007081hg38UCSC Ensembl
chr16:65980895..66040984hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3860090
hg1960090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499561
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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