A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933209



Internal ID22708518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26122705..26123153hg38UCSC Ensembl
chr13:26696843..26697291hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374818
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933209
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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