A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540300



Internal ID315088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95169920..95169947hg38UCSC Ensembl
chr14:95636257..95636284hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697702
Samples
Known GenesDICER1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540300
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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