A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492366



Internal ID269581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74853525..74854028hg38UCSC Ensembl
chr9:77468441..77468944hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024346
Samples
Known GenesTRPM6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492366
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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