A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282587



Internal ID20491805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:90205009..90205244hg38UCSC Ensembl
chr3:90254159..90254394hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744816
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282587
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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