A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933145



Internal ID22708453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111697177..111697284hg38UCSC Ensembl
chr13:112349524..112349631hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358706
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933145
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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