A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022775



Internal ID21932118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124281023..124281106hg38UCSC Ensembl
chr12:124765569..124765652hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617425
Samples
Known GenesZNF664-FAM101A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022775
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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