A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14462843



Internal ID22198042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66250101..66253619hg38UCSC Ensembl
chr11:66017572..66021090hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383519
hg193519
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3555201
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14462843
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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