A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756150



Internal ID20532010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154958491..154958491hg38UCSC Ensembl
chr5:154338051..154338051hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg382498
hg192498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289524
Samples
Known GenesMRPL22
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756150
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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