A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218361



Internal ID20785401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90713428..90735259hg38UCSC Ensembl
chr8:91725656..91747487hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3821832
hg1921832
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418424
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218361
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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