A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519093



Internal ID20892454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22703977..22706733hg38UCSC Ensembl
chr20:22684615..22687371hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg382757
hg192757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066818
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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