A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022853



Internal ID21932196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42206552..42207831hg38UCSC Ensembl
chr12:42600354..42601633hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg381280
hg191280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604297
Samples
Known GenesYAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022853
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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