A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526093



Internal ID20899454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22794895..22884991hg38UCSC Ensembl
chr20:22775533..22865629hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3890097
hg1990097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526093
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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