A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182628



Internal ID20749668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24378452..24384769hg38UCSC Ensembl
chr16:24389773..24396090hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg386318
hg196318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507640
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182628
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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