A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227803



Internal ID20794843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19908301..19911600hg38UCSC Ensembl
chr8:19765812..19769111hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429173
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227803
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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