A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593649



Internal ID20966720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55185376..55186004hg38UCSC Ensembl
chr14:55652094..55652722hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237812
Samples
Known GenesDLGAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593649
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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