A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543721



Internal ID21868076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98658652..98658652hg38UCSC Ensembl
chr4:99579803..99579803hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6071116
Supporting Variants
Samples
Known GenesTSPAN5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543721
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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