A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519369



Internal ID295721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36513267..36513576hg38UCSC Ensembl
chr20:35141670..35141979hg19UCSC 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 Variantsnssv17732198
Samples
Known GenesDLGAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519369
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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