A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992635



Internal ID21901978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183017581..183018454hg38UCSC Ensembl
chr3:182735369..182736242hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554933
Samples
Known GenesMCCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992635
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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