A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591951



Internal ID20965022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52716714..52717518hg38UCSC Ensembl
chr14:53183432..53184236hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38805
hg19805
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230259
Samples
Known GenesPSMC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591951
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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