A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544768



Internal ID21869123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113947606..113947606hg38UCSC Ensembl
chr4:114868762..114868762hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061068
Supporting Variants
Samples
Known GenesARSJ
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544768
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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