A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055898



Internal ID21965131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36415255..36427196hg38UCSC Ensembl
chr20:35043658..35055599hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3811942
hg1911942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637371
Samples
Known GenesDLGAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055898
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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