A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533624



Internal ID20906985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:687644..692940hg38UCSC Ensembl
chr20:668288..673584hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg385297
hg195297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070338
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533624
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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