A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591730



Internal ID20964801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43383460..43383943hg38UCSC Ensembl
chr11:43405010..43405493hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226807
Samples
Known GenesTTC17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591730
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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