A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053437



Internal ID21962670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51926583..52027660hg38UCSC Ensembl
chr20:50543122..50644199hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38101078
hg19101078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622979
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053437
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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