A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533549



Internal ID21857905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238398003..238398003hg38UCSC Ensembl
chr2:239306644..239306644hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054574
Supporting Variants
Samples
Known GenesTRAF3IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533549
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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