A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914373



Internal ID22689590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132723215..132723267hg38UCSC Ensembl
chr9:135598602..135598654hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914373
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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