A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14444559



Internal ID22226802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63082393..63083367hg38UCSC Ensembl
chr15:63374592..63375566hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38975
hg19975
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3244228
Supporting Variants
SamplesHG00733
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)nssv14444559
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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