A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526293



Internal ID20899654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24684300..24694449hg38UCSC Ensembl
chr20:24664936..24675085hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3810150
hg1910150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067128
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526293
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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