A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036105



Internal ID91814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52402676..52402727hg38UCSC Ensembl
chr10:54162436..54162487hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5410822
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036105
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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