A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100493



Internal ID22009726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79408790..79408790hg38UCSC Ensembl
chr18:77168790..77168790hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621644
Samples
Known GenesNFATC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100493
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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