A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524713



Internal ID300909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33006984..33007844hg38UCSC Ensembl
chr20:31594790..31595650hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38861
hg19861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731997
Samples
Known GenesBPIFB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524713
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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