A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982876



Internal ID21892219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23409658..23411267hg38UCSC Ensembl
chr1:23736151..23737760hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381610
hg191610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528437
Samples
Known GenesTCEA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982876
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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