A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139969



Internal ID339160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194515252..194551437hg38UCSC Ensembl
chr3:194235981..194272166hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3836186
hg1936186
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv362n206
Supporting Variantsnssv16944528
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139969
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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