A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596387



Internal ID21788430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119052397..119052397hg38UCSC Ensembl
chr10:120811909..120811909hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6082831
Supporting Variants
Samples
Known GenesEIF3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596387
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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