A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633986



Internal ID21582291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154958481..154958481hg38UCSC Ensembl
chr5:154338041..154338041hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg382755
hg192755
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124595
SamplesHG01505
Known GenesMRPL22
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633986
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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