A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098843



Internal ID22008076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64589323..64589323hg38UCSC Ensembl
chr12:64983103..64983103hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098843
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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