A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866096



Internal ID22641031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122231563..122235762hg38UCSC Ensembl
chr12:122716110..122720309hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469527
Samples
Known GenesVPS33A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866096
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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