A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588105



Internal ID20961176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108100540..108102351hg38UCSC Ensembl
chr11:107971267..107973078hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381812
hg191812
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1310n223
Supporting Variantsnssv18225127
Samples
Known GenesCUL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588105
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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