A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181568



Internal ID20748608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:43618047..43659709hg38UCSC Ensembl
chr18:41198012..41239674hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3841663
hg1941663
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181568
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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