A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580669



Internal ID20953740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80369039..80370660hg38UCSC Ensembl
chr11:80080083..80081704hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381622
hg191622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580669
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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