A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587766



Internal ID20960837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6462584..6462915hg38UCSC Ensembl
chr11:6483814..6484145hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218059
Samples
Known GenesTRIM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587766
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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