A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17527372



Internal ID21851729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99698773..99719572hg38UCSC Ensembl
chr2:100315235..100336034hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3820800
hg1920800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990913
Supporting Variants
Samples
Known GenesAFF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17527372
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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