A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094878



Internal ID22004111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109449831..109449831hg38UCSC Ensembl
chr12:109887636..109887636hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615065
Samples
Known GenesKCTD10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094878
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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