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nsv5538198

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 16 studies. See in: genome view    
Submitted genomic68,472,814-68,472,839Question Mark
Overlapping variant regions from other studies: 103 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):66,468,955-66,468,980Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5538198Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1768,472,81468,472,839
nsv5538198RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1766,468,95566,468,980

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714223insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714223Submitted genomicNC_000017.11:g.684
72814_68472839ins3
29
GRCh38 (hg38)NC_000017.11Chr1768,472,81468,472,839
nssv17714223RemappedPerfectNC_000017.10:g.664
68955_66468980ins3
29
GRCh37.p13First PassNC_000017.10Chr1766,468,95566,468,980

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)
nssv177142230.0221416366
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