A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222893



Internal ID20789933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114080624..114141672hg38UCSC Ensembl
chr8:115092853..115153901hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3861049
hg1961049
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419288
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222893
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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