A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484183



Internal ID261602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94643693..94761824hg38UCSC Ensembl
chr10:96403450..96521581hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38118132
hg19118132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036526
Samples
Known GenesCYP2C18
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484183
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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