A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5396641



Internal ID176056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80083547..80083598hg38UCSC Ensembl
chr8:80995782..80995833hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013330
Samples
Known GenesTPD52
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5396641
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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