A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263038



Internal ID20472256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86758340..86758396hg38UCSC Ensembl
chr9:89373255..89373311hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263038
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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