A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228757



Internal ID20795797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100728939..100746979hg38UCSC Ensembl
chr8:101741167..101759207hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3818041
hg1918041
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426758
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228757
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00051


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