A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995272



Internal ID21904615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150635697..150665079hg38UCSC Ensembl
chr4:151556849..151586231hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3829383
hg1929383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551231
Samples
Known GenesLRBA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995272
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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