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nsv5402108

  • 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: 86 SVs from 24 studies. See in: genome view    
Submitted genomic122,865,765-122,865,816Question Mark
Overlapping variant regions from other studies: 86 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):125,628,044-125,628,095Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5402108Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9122,865,765122,865,816
nsv5402108RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9125,628,044125,628,095

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17027130alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17027130Submitted genomicNC_000009.12:g.122
865765_122865816in
s250
GRCh38 (hg38)NC_000009.12Chr9122,865,765122,865,816
nssv17027130RemappedPerfectNC_000009.11:g.125
628044_125628095in
s250
GRCh37.p13First PassNC_000009.11Chr9125,628,044125,628,095

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)
nssv17027130<0.00156404
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