A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042531



Internal ID20609571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55931348..55931906hg38UCSC Ensembl
chr18:53598579..53599137hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524852
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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