A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5401020



Internal ID180397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90337521..90337572hg38UCSC Ensembl
chr8:91349749..91349800hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17014991
Samples
Known GenesLINC00534
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5401020
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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