A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210639



Internal ID20777679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:90248401..90297900hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3849500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342033
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210639
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00411


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