A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920099



Internal ID22695322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121747448..121762951hg38UCSC Ensembl
chr8:122759688..122775191hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3815504
hg1915504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920099
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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