A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995493



Internal ID21904836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154610942..154611854hg38UCSC Ensembl
chr4:155532094..155533006hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552584
Samples
Known GenesFGG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995493
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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