A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590329



Internal ID20963400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130041192..130041992hg38UCSC Ensembl
chr11:129911087..129911887hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590329
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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