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nsv5480298

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,393

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 205 SVs from 29 studies. See in: genome view    
Submitted genomic103,396,266-103,398,658Question Mark
Overlapping variant regions from other studies: 205 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):104,408,494-104,410,886Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5480298Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8103,396,266103,398,658
nsv5480298RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8104,408,494104,410,886

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17014298deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17014298Submitted genomicNC_000008.11:g.103
396266_103398658de
l
GRCh38 (hg38)NC_000008.11Chr8103,396,266103,398,658
nssv17014298RemappedPerfectNC_000008.10:g.104
408494_104410886de
l
GRCh37.p13First PassNC_000008.10Chr8104,408,494104,410,886

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)
nssv17014298<0.00116404
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