A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765122



Internal ID20540982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63546581..63546581hg38UCSC Ensembl
chr20:62177934..62177934hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268477
Samples
Known GenesSRMS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765122
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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