A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992190



Internal ID21901533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183957399..183957557hg38UCSC Ensembl
chr3:183675187..183675345hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553915
Samples
Known GenesABCC5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992190
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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