A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485078



Internal ID262475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96596494..96598501hg38UCSC Ensembl
chr10:98356251..98358258hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382008
hg192008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039744
Samples
Known GenesPIK3AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485078
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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