A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045215



Internal ID21954485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:166336687..166336687hg38UCSC Ensembl
chr2:167193197..167193197hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526190
Samples
Known GenesSCN9A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045215
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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