A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469309



Internal ID247098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110554735..110566697hg38UCSC Ensembl
chr6:110875938..110887900hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3811963
hg1911963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469309
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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