A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590226



Internal ID20963297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21345879..21346549hg38UCSC Ensembl
chr14:21814038..21814708hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230166
Samples
Known GenesRPGRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590226
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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