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nsv5447108

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,254

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 84 SVs from 17 studies. See in: genome view    
Submitted genomic69,562,811-69,564,064Question Mark
Overlapping variant regions from other studies: 84 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):69,789,943-69,791,196Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5447108Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr269,562,81169,564,064
nsv5447108RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr269,789,94369,791,196

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17725898deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17725898Submitted genomicNC_000002.12:g.695
62811_69564064del
GRCh38 (hg38)NC_000002.12Chr269,562,81169,564,064
nssv17725898RemappedPerfectNC_000002.11:g.697
89943_69791196del
GRCh37.p13First PassNC_000002.11Chr269,789,94369,791,196

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)
nssv17725898<0.00116404
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