A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885294



Internal ID22660278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43947186..43958198hg38UCSC Ensembl
chr22:44343066..44354078hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3811013
hg1911013
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484172
Samples
Known GenesPNPLA3, SAMM50
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885294
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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