A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530698



Internal ID20904059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6797586..6822266hg38UCSC Ensembl
chr20:6778233..6802913hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3824681
hg1924681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204074
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530698
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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