A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352400



Internal ID21009953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:90234401..90334800hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38100400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4032n223
Supporting Variantsnssv18210612
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352400
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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