A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914811



Internal ID22690028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87401526..87402413hg38UCSC Ensembl
chr9:90016441..90017328hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38888
hg19888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914811
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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