A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3235958



Internal ID22373448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100104633..100104767hg38UCSC Ensembl
chr4:101025790..101025924hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14315445
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3235958
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