A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031692



Internal ID88842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:41699000..41916000hg38UCSC Ensembl
chr10:42354936..42541209hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38217001
hg19186274
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485916
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031692
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001881


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