A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460103



Internal ID238098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13753949..13756239hg38UCSC Ensembl
chr6:13754181..13756471hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg382291
hg192291
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980996
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460103
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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