A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059063



Internal ID21968296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56515592..56515661hg38UCSC Ensembl
chr20:55090648..55090717hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622858
Samples
Known GenesGCNT7, RTFDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059063
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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