A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110605



Internal ID22019838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53050109..53050109hg38UCSC Ensembl
chr20:51666648..51666648hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634145
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110605
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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