A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032182



Internal ID89159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22882955..22889144hg38UCSC Ensembl
chr10:23171884..23178073hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg386190
hg196190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474281
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032182
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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