A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492240



Internal ID269457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94318000..94352552hg38UCSC Ensembl
chr9:97080282..97114834hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3834553
hg1934553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025757
Samples
Known GenesLOC100132077, NUTM2F
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492240
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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