A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484335



Internal ID261748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96346595..96346790hg38UCSC Ensembl
chr10:98106352..98106547hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038793
Samples
Known GenesOPALIN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484335
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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