A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140266



Internal ID339459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197032451..197034959hg38UCSC Ensembl
chr3:196759322..196761830hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382509
hg192509
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16946031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140266
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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