A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3242334



Internal ID22375242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66054085..66054229hg38UCSC Ensembl
chr9:42467094..42467238hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14428736
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsInsertion variant involving HSAT satellite DNA
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3242334
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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