A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235151



Internal ID20802191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89673133..89709166hg38UCSC Ensembl
chr8:90685361..90721394hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3836034
hg1936034
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435184
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235151
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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