A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139446



Internal ID338631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98406381..98412480hg38UCSC Ensembl
chr3:98125225..98131324hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139446
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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