A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024291



Internal ID21933634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120478059..120481011hg38UCSC Ensembl
chr12:120915862..120918814hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg382953
hg192953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612035
Samples
Known GenesDYNLL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024291
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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