A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079289



Internal ID21988522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46375854..46375854hg38UCSC Ensembl
chr4:46377871..46377871hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551399
Samples
Known GenesGABRA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079289
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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