A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209280



Internal ID20776320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46244468..46246354hg38UCSC Ensembl
chr3:46285959..46287845hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381887
hg191887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362529
Supporting Variants
Samples
Known GenesCCR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209280
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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