A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852813



Internal ID22627748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67561131..67564247hg38UCSC Ensembl
chr10:69320889..69324005hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383117
hg193117
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450096
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852813
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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