A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532035



Internal ID21856391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113948974..113948974hg38UCSC Ensembl
chr2:114706551..114706551hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg383883
hg193883
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056945
Supporting Variants
Samples
Known GenesACTR3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532035
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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