A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274017



Internal ID20483235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63294069..63294069hg38UCSC Ensembl
chr20:61925421..61925421hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753115
Supporting Variants
Samples
Known GenesCOL20A1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274017
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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