A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853940



Internal ID22628875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111534043..111537326hg38UCSC Ensembl
chr12:111971847..111975130hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg383284
hg193284
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453431
Samples
Known GenesATXN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853940
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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