A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583826



Internal ID20956897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13722536..13723228hg38UCSC Ensembl
chr11:13744083..13744775hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38693
hg19693
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218878
Samples
Known GenesFAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583826
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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