A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592988



Internal ID20966059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107934930..107935055hg38UCSC Ensembl
chr11:107805656..107805781hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219305
Samples
Known GenesRAB39A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592988
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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