A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577291



Internal ID20950362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43462927..43464242hg38UCSC Ensembl
chr11:43484477..43485792hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218741
Samples
Known GenesTTC17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577291
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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