A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083484



Internal ID21992717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114733564..114733564hg38UCSC Ensembl
chr12:115171369..115171369hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083484
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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