A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533767



Internal ID20907128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22934501..22941800hg38UCSC Ensembl
chr20:22915138..22922437hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066834
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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