A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182583



Internal ID20749623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:43132010..43162335hg38UCSC Ensembl
chr18:40711975..40742300hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3830326
hg1930326
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534547
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182583
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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