A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097891



Internal ID22007124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78108788..78108788hg38UCSC Ensembl
chr17:76104869..76104869hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629378
Samples
Known GenesTNRC6C, TNRC6C-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097891
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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