A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553689



Internal ID21878044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17272841..17272841hg38UCSC Ensembl
chr3:17314333..17314333hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057357
Supporting Variants
Samples
Known GenesTBC1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553689
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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