A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17012136



Internal ID75760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74074436..74091107hg38UCSC Ensembl
chr8:74986671..75003342hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3816672
hg1916672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479852
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17012136
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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