A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189695



Internal ID20756735
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 StatusS
Merged Variantsnsv6500074
Supporting Variants
Samples
Known GenesMLKL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189695
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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