A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559673



Internal ID332700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95174989..95175040hg38UCSC Ensembl
chr14:95641326..95641377hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697703
Samples
Known GenesDICER1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559673
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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