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nsv5421739

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 356 SVs from 58 studies. See in: genome view    
Submitted genomic18,425,014-18,425,065Question Mark
Overlapping variant regions from other studies: 356 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):18,328,328-18,328,379Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5421739Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1718,425,01418,425,065
nsv5421739RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1718,328,32818,328,379

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17711926alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17711926Submitted genomicNC_000017.11:g.184
25014_18425065ins2
80
GRCh38 (hg38)NC_000017.11Chr1718,425,01418,425,065
nssv17711926RemappedPerfectNC_000017.10:g.183
28328_18328379ins2
80
GRCh37.p13First PassNC_000017.10Chr1718,328,32818,328,379

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)
nssv17711926<0.00126404
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