A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098913



Internal ID22008146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116735574..116735574hg38UCSC Ensembl
chr12:117173379..117173379hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598292
Samples
Known GenesC12orf49
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098913
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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