A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16911874



Internal ID8675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38297659..38299719hg38UCSC Ensembl
chr2:38524801..38526861hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg382061
hg192061
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562590
Supporting Variants
Samples
Known GenesATL2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16911874
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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