A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238381



Internal ID20805421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95144266..95144385hg38UCSC Ensembl
chr14:95610603..95610722hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584694
Supporting Variants
Samples
Known GenesDICER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238381
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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