A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028458



Internal ID21937801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76120570..76122633hg38UCSC Ensembl
chr12:76514350..76516413hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg382064
hg192064
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605621
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028458
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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