A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035140



Internal ID91162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69563505..69563581hg38UCSC Ensembl
chr10:71323261..71323337hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483165
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035140
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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