A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3244538



Internal ID22375888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63082393..63083336hg38UCSC Ensembl
chr15:63374592..63375535hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38944
hg19944
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2955n152
Supporting Variantsnssv14377843
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsInsertion variant involving LTR satellite DNA
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3244538
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