A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040113



Internal ID94458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129395684..129395684hg38UCSC Ensembl
chr10:131193948..131193948hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538479
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040113
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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