A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526461



Internal ID20899822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31181137..31229454hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3848318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202653
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526461
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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