A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919321



Internal ID22694543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83587488..83591547hg38UCSC Ensembl
chr9:86202403..86206462hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg384060
hg194060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440888
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919321
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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