A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625121



Internal ID21817168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62830653..62830653hg38UCSC Ensembl
chr20:61462005..61462005hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102124
Supporting Variants
Samples
Known GenesCOL9A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625121
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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