A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576117



Internal ID20949188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8119377..8135412hg38UCSC Ensembl
chr11:8140924..8156959hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3816036
hg1916036
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218462
Samples
Known GenesRIC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576117
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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