A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523508



Internal ID21847867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99082099..99082099hg38UCSC Ensembl
chr2:99698562..99698562hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047245
Supporting Variants
Samples
Known GenesTSGA10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523508
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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