A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588845



Internal ID20961916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35288702..35318244hg38UCSC Ensembl
chr14:35757908..35787450hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3829543
hg1929543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222633
Samples
Known GenesPSMA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588845
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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