A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591186



Internal ID20964257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73085311..73141884hg38UCSC Ensembl
chr14:73552019..73608592hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3856574
hg1956574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238637
Samples
Known GenesPSEN1, RBM25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591186
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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