A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434825



Internal ID213492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127840661..127840716hg38UCSC Ensembl
chr3:127559504..127559559hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434825
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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