A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554108



Internal ID20927217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43325711..43326377hg38UCSC Ensembl
chr20:41954351..41955017hg19UCSC Ensembl
Cytoband20q13.11
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554108
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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