A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139947



Internal ID339138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39644041..39648086hg38UCSC Ensembl
chr3:39685532..39689577hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg384046
hg194046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139947
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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