A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276711



Internal ID20485929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99313938..99313995hg38UCSC Ensembl
chr9:102076220..102076277hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736472
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276711
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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