A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468814



Internal ID246605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106101381..106128000hg38UCSC Ensembl
chr4:107022538..107049157hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3826620
hg1926620
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16955417
Samples
Known GenesTBCK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468814
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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