A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3557363



Internal ID22426169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207645319..207645513hg38UCSC Ensembl
chr2:208510043..208510237hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14295081, nssv14295078, nssv14295083, nssv14295084, nssv14295082, nssv14295086, nssv14295085, nssv14295079, nssv14295080
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3557363
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