A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107781



Internal ID22017014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63956543..63956543hg38UCSC Ensembl
chr20:62587896..62587896hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646214
Samples
Known GenesUCKL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107781
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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