A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590366



Internal ID20963437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80607026..80736020hg38UCSC Ensembl
chr11:80318070..80447063hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38128995
hg19128994
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220472
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590366
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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