A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926882



Internal ID22702110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94147593..94155379hg38UCSC Ensembl
chr9:96909875..96917661hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg387787
hg197787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444752
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926882
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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