A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141504



Internal ID340701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60664000..60673000hg38UCSC Ensembl
chr9_gl000199_random:145442..154442hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg389001
hg199001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141504
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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