A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226652



Internal ID20793692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100877814..100918438hg38UCSC Ensembl
chr8:101890042..101930666hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3840625
hg1940625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430070
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226652
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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