A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053451



Internal ID21962684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61348678..61354650hg38UCSC Ensembl
chr20:59923734..59929706hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385973
hg195973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617584
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053451
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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