A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196057



Internal ID20763097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:43685342..43719237hg38UCSC Ensembl
chr18:41265307..41299202hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3833896
hg1933896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534999
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196057
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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