A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220271



Internal ID20787311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:82993889..83086997hg38UCSC Ensembl
chr8:83906124..83999232hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3893109
hg1993109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220271
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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