A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584051



Internal ID20957122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43558173..43568370hg38UCSC Ensembl
chr11:43579723..43589920hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3810198
hg1910198
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218957
Samples
Known GenesMIR670
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584051
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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