A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036231



Internal ID91899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59008325..59008452hg38UCSC Ensembl
chr10:60768085..60768212hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482852
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036231
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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