A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206268



Internal ID20773308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224529522..224530132hg38UCSC Ensembl
chr2:225394239..225394849hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344705
Supporting Variants
Samples
Known GenesCUL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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