A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102798



Internal ID22012032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59843241..59843241hg38UCSC Ensembl
chr20:58418296..58418296hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625691
Samples
Known GenesPHACTR3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102798
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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