A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040056



Internal ID20607096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38486615..38492008hg38UCSC Ensembl
chr18:36066579..36071972hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg385394
hg195394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522309
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040056
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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