A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551268



Internal ID21875623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193803697..193803697hg38UCSC Ensembl
chr3:193521486..193521486hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6078041
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551268
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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