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nsv5489363

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:368

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 118 SVs from 27 studies. See in: genome view    
Submitted genomic68,495,325-68,495,692Question Mark
Overlapping variant regions from other studies: 118 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):70,255,082-70,255,449Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5489363Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1068,495,32568,495,692
nsv5489363RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1070,255,08270,255,449

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17037449duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17037449Submitted genomicNC_000010.11:g.684
95325_68495692dup
GRCh38 (hg38)NC_000010.11Chr1068,495,32568,495,692
nssv17037449RemappedPerfectNC_000010.10:g.702
55082_70255449dup
GRCh37.p13First PassNC_000010.10Chr1070,255,08270,255,449

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)
nssv17037449<0.00116404
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