A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553393



Internal ID21877748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182232622..182232622hg38UCSC Ensembl
chr3:181950410..181950410hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553393
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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