A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988014



Internal ID21897357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23348205..23348268hg38UCSC Ensembl
chr2:23571076..23571139hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988014
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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