A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202544



Internal ID22351694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126473080..126473131hg38UCSC Ensembl
chr11:126342975..126343026hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1619n152
Supporting Variantsnssv14443832
SamplesHG00733
Known GenesKIRREL3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202544
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