A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3231467



Internal ID22372241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69176999..69182944hg38UCSC Ensembl
chr11:68944467..68950412hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg385946
hg195946
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357077, nssv14357076, nssv14357078, nssv14357081, nssv14357079, nssv14357080
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3231467
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