A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863858



Internal ID22638793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120523184..120524583hg38UCSC Ensembl
chr12:120960987..120962386hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455922
Samples
Known GenesCOQ5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863858
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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