A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477858



Internal ID255424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125106647..125106775hg38UCSC Ensembl
chr9:127868926..127869054hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027224
Samples
Known GenesSCAI
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477858
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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