A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465232



Internal ID243100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141748790..141818790hg38UCSC Ensembl
chr6:142069927..142139927hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3870001
hg1970001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16971173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465232
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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