A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920081



Internal ID22695304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99408780..99408919hg38UCSC Ensembl
chr9:102171062..102171201hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443768
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920081
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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