A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922269



Internal ID15600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:172227065..172228997hg38UCSC Ensembl
chr2:173091793..173093725hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381933
hg191933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438695
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922269
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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