A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058104



Internal ID21967338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63034927..63035107hg38UCSC Ensembl
chr20:61666279..61666459hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627574
Samples
Known GenesLINC00029, LOC63930
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058104
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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