A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478024



Internal ID255588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93511189..93512381hg38UCSC Ensembl
chr9:96273471..96274663hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381193
hg191193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738500
Samples
Known GenesFAM120A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478024
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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