A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926163



Internal ID22701390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98024274..98027013hg38UCSC Ensembl
chr9:100786556..100789295hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382740
hg192740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926163
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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