A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061432



Internal ID21970665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174787498..174787498hg38UCSC Ensembl
chr4:175708649..175708649hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543543
Samples
Known GenesGLRA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061432
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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