A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488871



Internal ID266165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67494465..67494899hg38UCSC Ensembl
chr10:69254223..69254657hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037326
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488871
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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