A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3548826



Internal ID22417778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126276308..126276308hg38UCSC Ensembl
chr11:126146203..126146203hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382175
hg192175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14443830
SamplesHG00733
Known GenesFOXRED1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3548826
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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