A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236062



Internal ID20803102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92767300..92822014hg38UCSC Ensembl
chr8:93779528..93834242hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3854715
hg1954715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417716
Supporting Variants
Samples
Known GenesFLJ46284
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236062
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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