A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766432



Internal ID20542292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128286089..128286089hg38UCSC Ensembl
chr4:129207244..129207244hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269764
Samples
Known GenesPGRMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766432
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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