A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139730



Internal ID338919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32765254..32766569hg38UCSC Ensembl
chr3:32806746..32808061hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932373
Samples
Known GenesCNOT10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139730
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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