A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141620



Internal ID340817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65182450..65235082hg38UCSC Ensembl
chr9:70076056..70128688hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3852633
hg1952633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141620
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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