A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501911



Internal ID278797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112036688..112044379hg38UCSC Ensembl
chr13:112691002..112698693hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg387692
hg197692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17692762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501911
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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