A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915143



Internal ID22690361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107564090..107564923hg38UCSC Ensembl
chr9:110326371..110327204hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38834
hg19834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433347
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915143
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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