A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020694



Internal ID21930037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108436445..108437402hg38UCSC Ensembl
chr12:108830222..108831179hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38958
hg19958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11n212
Supporting Variantsnssv17599653
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020694
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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