A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533974



Internal ID309838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101016989..101017039hg38UCSC Ensembl
chr8:102029217..102029267hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17014746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533974
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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