A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020722



Internal ID21930065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:43685620..43685749hg38UCSC Ensembl
chr12:44079423..44079552hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020722
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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