A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222770



Internal ID20789810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89981901..89989400hg38UCSC Ensembl
chr8:90994129..91001628hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430268
Supporting Variants
Samples
Known GenesNBN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222770
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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