A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580966



Internal ID20954037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130011055..130011822hg38UCSC Ensembl
chr11:129880950..129881717hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230655
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580966
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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