A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284041



Internal ID20493259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62166677..62166677hg38UCSC Ensembl
chr20:60741733..60741733hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759344
Supporting Variants
Samples
Known GenesSS18L1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284041
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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