A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059202



Internal ID21968436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38510617..38510926hg38UCSC Ensembl
chr20:37139260..37139569hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629271
Samples
Known GenesRALGAPB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059202
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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