A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522942



Internal ID20896303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17976277..17976495hg38UCSC Ensembl
chr20:17956920..17957138hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066668
Samples
Known GenesMGME1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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