A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139900



Internal ID339090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132945787..132951574hg38UCSC Ensembl
chr3:132664631..132670418hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg385788
hg195788
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139900
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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