A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052014



Internal ID21961247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:166334482..166334482hg38UCSC Ensembl
chr2:167190992..167190992hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518076
Samples
Known GenesSCN9A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052014
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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