A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196726



Internal ID20763766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:76597419..76608966hg38UCSC Ensembl
chr16:76631316..76642863hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3811548
hg1911548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500254
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196726
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00242


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