A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3548286



Internal ID22417243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197786515..197789904hg38UCSC Ensembl
chr1:197755645..197759034hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg383390
hg193390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14467276
SamplesHG00731
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3548286
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