A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039024



Internal ID21948367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119198238..119200065hg38UCSC Ensembl
chr12:119636043..119637870hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg381828
hg191828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039024
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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