A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448989



Internal ID22506859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90048959..90049137hg38UCSC Ensembl
chr9:92811241..92811419hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910874
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448989
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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