A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14392049



Internal ID22289497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116394452..116394584hg38UCSC Ensembl
chr10:118153964..118154096hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3246174
Supporting Variants
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)nssv14392049
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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