A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915158



Internal ID22690376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130260411..130315947hg38UCSC Ensembl
chr9:133022690..133073060hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3855537
hg1950371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440367
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915158
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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