A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449450



Internal ID22507320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116135172..116140399hg38UCSC Ensembl
chr9:118897451..118902678hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg385228
hg195228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920628
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449450
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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