A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584237



Internal ID20957308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65101763..65102085hg38UCSC Ensembl
chr11:64869235..64869557hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235782
Samples
Known GenesVPS51
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584237
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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