A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352476



Internal ID21010029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216718399..216751003hg38UCSC Ensembl
chr2:217583122..217615726hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3832605
hg1932605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352476
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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