A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909389



Internal ID22684599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97974476..97977444hg38UCSC Ensembl
chr9:100736758..100739726hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382969
hg192969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909389
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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