A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520778



Internal ID20894139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:8870774..8915458hg38UCSC Ensembl
chr20:8851421..8896105hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3844685
hg1944685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202996
Samples
Known GenesPLCB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520778
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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