A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041076



Internal ID95090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110468101..110469551hg38UCSC Ensembl
chr10:112227859..112229309hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381451
hg191451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497683
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041076
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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