A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3243764



Internal ID22375665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:73129303..73137504hg38UCSC Ensembl
chr1:73594986..73603187hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg388202
hg198202
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv274n152
Supporting Variantsnssv14413199
SamplesHG00514
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)nsv3243764
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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