A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584694



Internal ID20957765
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 StatusM
Merged Variants
Supporting Variantsnssv18238381
Samples
Known GenesDICER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584694
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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