A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881100



Internal ID22656073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59033327..59035545hg38UCSC Ensembl
chr20:57608382..57610600hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg382219
hg192219
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486736
Samples
Known GenesSLMO2, SLMO2-ATP5E
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881100
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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