A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208079



Internal ID20775119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203384346..203385170hg38UCSC Ensembl
chr2:204249069..204249893hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38825
hg19825
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351657
Supporting Variants
Samples
Known GenesABI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208079
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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