A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861426



Internal ID22636361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93431336..93435188hg38UCSC Ensembl
chr12:93825112..93828964hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg383853
hg193853
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463541
Samples
Known GenesUBE2N
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861426
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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