A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207958



Internal ID20774998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123201601..123202800hg38UCSC Ensembl
chr3:122920448..122921647hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374822
Supporting Variants
Samples
Known GenesSEC22A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207958
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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