A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289145



Internal ID20498363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134415901..134415901hg38UCSC Ensembl
chr3:134134743..134134743hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759422
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289145
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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