A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035865



Internal ID91653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59941474..59949282hg38UCSC Ensembl
chr10:61701232..61709040hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg387809
hg197809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488620
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035865
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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