A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039485



Internal ID21948828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106896610..106896779hg38UCSC Ensembl
chr12:107290388..107290557hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597798
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039485
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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