A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139997



Internal ID339189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99327644..99332500hg38UCSC Ensembl
chr3:99046488..99051344hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg384857
hg194857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734889
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139997
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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