A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629271



Internal ID21821318
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 StatusS
Merged Variantsnsv6059202
Supporting Variants
Samples
Known GenesRALGAPB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629271
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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