A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518229



Internal ID20891590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32471338..32474851hg38UCSC Ensembl
chr20:31059141..31062654hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg383514
hg193514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067391
Samples
Known GenesC20orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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