A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532773



Internal ID21857129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25723191..25723314hg38UCSC Ensembl
chr2:25946060..25946183hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5988816
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532773
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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