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nsv5491103

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:891

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 137 SVs from 33 studies. See in: genome view    
Submitted genomic130,777,444-130,778,334Question Mark
Overlapping variant regions from other studies: 137 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):133,652,831-133,653,721Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5491103Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9130,777,444130,778,334
nsv5491103RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9133,652,831133,653,721

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17028900deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17028900Submitted genomicNC_000009.12:g.130
777444_130778334de
l
GRCh38 (hg38)NC_000009.12Chr9130,777,444130,778,334
nssv17028900RemappedPerfectNC_000009.11:g.133
652831_133653721de
l
GRCh37.p13First PassNC_000009.11Chr9133,652,831133,653,721

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)
nssv170289000.002116400
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