A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437346



Internal ID22495216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21950596..21952634hg38UCSC Ensembl
chr9:21950595..21952633hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg382039
hg192039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908374
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437346
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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