A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084649



Internal ID21993882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109106906..109106906hg38UCSC Ensembl
chr12:109544711..109544711hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614463
Samples
Known GenesUNG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084649
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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