A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053658



Internal ID21962891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25364155..25368775hg38UCSC Ensembl
chr20:25344791..25349411hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg384621
hg194621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624838
Samples
Known GenesABHD12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053658
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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