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nsv5526860

  • 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: 165 SVs from 28 studies. See in: genome view    
Submitted genomic40,978,598-40,978,649Question Mark
Overlapping variant regions from other studies: 163 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):39,134,850-39,134,901Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5526860Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1740,978,59840,978,649
nsv5526860RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1739,134,85039,134,901

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713135deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713135Submitted genomicNC_000017.11:g.409
78598_40978649del
GRCh38 (hg38)NC_000017.11Chr1740,978,59840,978,649
nssv17713135RemappedPerfectNC_000017.10:g.391
34850_39134901del
GRCh37.p13First PassNC_000017.10Chr1739,134,85039,134,901

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)
nssv177131350.013816394
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