A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591391



Internal ID20964462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18623322..18645846hg38UCSC Ensembl
chr11:18644869..18667393hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3822525
hg1922525
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235521
Samples
Known GenesSPTY2D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591391
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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