A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523751



Internal ID21848110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26599891..26600222hg38UCSC Ensembl
chr2:26822759..26823090hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5988631
Supporting Variants
Samples
Known GenesCIB4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523751
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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