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nsv5553601

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 76 SVs from 16 studies. See in: genome view    
Submitted genomic38,786,586-38,786,624Question Mark
Overlapping variant regions from other studies: 76 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):39,182,591-39,182,629Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5553601Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2238,786,58638,786,624
nsv5553601RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2239,182,59139,182,629

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17728959insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17728959Submitted genomicNC_000022.11:g.387
86586_38786624ins3
25
GRCh38 (hg38)NC_000022.11Chr2238,786,58638,786,624
nssv17728959RemappedPerfectNC_000022.10:g.391
82591_39182629ins3
25
GRCh37.p13First PassNC_000022.10Chr2239,182,59139,182,629

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17728959<0.00116404
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