A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500074



Internal ID20873299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74678268..74693806hg38UCSC Ensembl
chr16:74712166..74727704hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3815539
hg1915539
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189695
Samples
Known GenesMLKL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500074
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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