A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3236594



Internal ID22373629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63082393..63083364hg38UCSC Ensembl
chr15:63374592..63375563hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2955n152
Supporting Variantsnssv14418261
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)nsv3236594
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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