A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561810



Internal ID21886165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158982048..158982048hg38UCSC Ensembl
chr5:158409056..158409056hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072547
Supporting Variants
Samples
Known GenesEBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561810
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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