A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524936



Internal ID301118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:13784358..13784536hg38UCSC Ensembl
chr20:13765004..13765182hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731023
Samples
Known GenesESF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524936
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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