A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161189



Internal ID21473314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16320341..16320433hg38UCSC Ensembl
chr9:16320339..16320431hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589426
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161189
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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