A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584143



Internal ID20957214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110358086..110359029hg38UCSC Ensembl
chr11:110228811..110229754hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38944
hg19944
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584143
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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