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nsv5482037

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 93 SVs from 23 studies. See in: genome view    
Submitted genomic92,670,549-92,670,612Question Mark
Overlapping variant regions from other studies: 93 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):95,432,831-95,432,894Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5482037Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr992,670,54992,670,612
nsv5482037RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr995,432,83195,432,894

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17738498deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17738498Submitted genomicNC_000009.12:g.926
70549_92670612del
GRCh38 (hg38)NC_000009.12Chr992,670,54992,670,612
nssv17738498RemappedPerfectNC_000009.11:g.954
32831_95432894del
GRCh37.p13First PassNC_000009.11Chr995,432,83195,432,894

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)
nssv17738498<0.00116404
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