A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033379



Internal ID20600419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85396854..85403931hg38UCSC Ensembl
chr16:85430460..85437537hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg387078
hg197078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511210
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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