A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535273



Internal ID20908634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16669243..16695857hg38UCSC Ensembl
chr20:16649888..16676502hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3826615
hg1926615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205231
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535273
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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