A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037111



Internal ID92502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80226368..80233000hg38UCSC Ensembl
chr10:81986124..81992756hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg386633
hg196633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483238
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037111
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000313


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