A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043362



Internal ID20610402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62410473..62415965hg38UCSC Ensembl
chr18:60077706..60083198hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg385493
hg195493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524581
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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