A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918175



Internal ID22693396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43154993..43161527hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918175
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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