A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219228



Internal ID20786268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36206238..36229032hg38UCSC Ensembl
chr8:36063756..36086550hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3822795
hg1922795
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426535
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219228
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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