A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097403



Internal ID22006636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21265374..21265374hg38UCSC Ensembl
chr14:21733533..21733533hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602660
Samples
Known GenesHNRNPC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097403
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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