A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071116



Internal ID21980349
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 StatusM
Merged Variants
Supporting Variantsnssv17543721
Samples
Known GenesTSPAN5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071116
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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