nsv5514994

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:98

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 106 SVs from 16 studies. See in: genome view    
Submitted genomic18,534,404-18,534,501Question Mark
Overlapping variant regions from other studies: 106 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):18,515,048-18,515,145Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514994Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2018,534,40418,534,501
nsv5514994RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2018,515,04818,515,145

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17731370deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17731370Submitted genomicNC_000020.11:g.185
34404_18534501del
GRCh38 (hg38)NC_000020.11Chr2018,534,40418,534,501
nssv17731370RemappedPerfectNC_000020.10:g.185
15048_18515145del
GRCh37.p13First PassNC_000020.10Chr2018,515,04818,515,145

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)
nssv17731370<0.00116404
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