A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3241770



Internal ID22375062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24219804..24219906hg38UCSC Ensembl
chr20:24200440..24200542hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14454461
SamplesHG00733
Known GenesFLJ33581
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsDeletion variant involving LTR satellite DNA
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3241770
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