A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040786



Internal ID94904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118280541..118283827hg38UCSC Ensembl
chr10:120040053..120043339hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383287
hg193287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507361
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040786
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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