A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578815



Internal ID20951886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18505865..18506534hg38UCSC Ensembl
chr11:18527412..18528081hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218436
Samples
Known GenesTSG101
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578815
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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