A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553866



Internal ID20926978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45916559..45926977hg38UCSC Ensembl
chr20:44545198..44555616hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3810419
hg1910419
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202903
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553866
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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