A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142435



Internal ID341635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41452504..41576504hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38124001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024874
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142435
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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