A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142566



Internal ID341767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60568000..60654100hg38UCSC Ensembl
chr9_gl000199_random:49442..135542hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3886101
hg1986101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142566
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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