A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732476



Internal ID20508400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112574886..112575162hg38UCSC Ensembl
chr12:113012690..113012966hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732476
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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