A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533438



Internal ID20906799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4188920..4190667hg38UCSC Ensembl
chr20:4169567..4171314hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381748
hg191748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533438
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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