A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14376442



Internal ID22327540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57322112..57322228hg38UCSC Ensembl
chr10:59081872..59081988hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3232544
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)nssv14376442
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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