A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636833



Internal ID21828880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6030923..6030923hg38UCSC Ensembl
chr20:6011569..6011569hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103578
Supporting Variants
Samples
Known GenesCRLS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636833
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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