A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3233589



Internal ID22372798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71568878..71579777hg38UCSC Ensembl
chr11:71279924..71290823hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3810900
hg1910900
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357793, nssv14357797, nssv14357796, nssv14357795, nssv14357794, nssv14357798
SamplesHG00512, HG00731, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3233589
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer