A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520842



Internal ID20894203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4576522..4585919hg38UCSC Ensembl
chr20:4557168..4566565hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg389398
hg199398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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