A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033469



Internal ID20600509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86299059..86299325hg38UCSC Ensembl
chr16:86332665..86332931hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512240
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00161


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