A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039339



Internal ID21948682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:47940862..47941325hg38UCSC Ensembl
chr12:48334645..48335108hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039339
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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