A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487461



Internal ID264799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124854856..124959719hg38UCSC Ensembl
chr8:125867098..125971961hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38104864
hg19104864
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17017158
Samples
Known GenesLINC00964
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487461
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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