A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559584



Internal ID20932655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138194654..138620353hg38UCSC Ensembl
chr7:137879400..138305098hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38425700
hg19425699
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274356
Samples
Known GenesSVOPL, TRIM24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559584
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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