A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029465



Internal ID20596505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24528401..24535300hg38UCSC Ensembl
chr16:24539722..24546621hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504551
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029465
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02618


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