A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548764



Internal ID20921946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43845701..43855400hg38UCSC Ensembl
chr20:42474341..42484040hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg389700
hg199700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4468n223
Supporting Variantsnssv18202872
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548764
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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