A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029106



Internal ID87102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10703262..10704817hg38UCSC Ensembl
chr10:10745225..10746780hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381556
hg191556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480317
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029106
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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