A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533066



Internal ID20906427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31459201..31468800hg38UCSC Ensembl
chr20:30047004..30056603hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067358
Samples
Known GenesDEFB124
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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