A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142522



Internal ID341722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40561974..41135974hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38574001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142522
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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