A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973509



Internal ID22748444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89511284..89511284hg38UCSC Ensembl
chr14:89977628..89977628hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383539
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973509
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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