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nsv5510830

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:60

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 131 SVs from 24 studies. See in: genome view    
Submitted genomic6,631,540-6,631,599Question Mark
Overlapping variant regions from other studies: 131 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):6,740,706-6,740,765Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5510830Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr126,631,5406,631,599
nsv5510830RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr126,740,7066,740,765

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17054694deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17054694Submitted genomicNC_000012.12:g.663
1540_6631599del
GRCh38 (hg38)NC_000012.12Chr126,631,5406,631,599
nssv17054694RemappedPerfectNC_000012.11:g.674
0706_6740765del
GRCh37.p13First PassNC_000012.11Chr126,740,7066,740,765

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)
nssv17054694<0.00116404
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