A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033470



Internal ID90002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29084631..29087278hg38UCSC Ensembl
chr10:29373560..29376207hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg382648
hg192648
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480407
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033470
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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