A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039385



Internal ID93978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120185627..120185776hg38UCSC Ensembl
chr10:121945139..121945288hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500868
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039385
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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