A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037927



Internal ID93035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93575172..93575223hg38UCSC Ensembl
chr10:95334929..95334980hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5398389
Supporting Variants
Samples
Known GenesFFAR4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037927
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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