A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162529



Internal ID21493376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87411712..87411772hg38UCSC Ensembl
chr9:90026627..90026687hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592687
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162529
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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