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nsv5549478

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 25 studies. See in: genome view    
Submitted genomic53,306,613-53,306,613Question Mark
Overlapping variant regions from other studies: 103 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):53,700,397-53,700,397Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5549478Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1253,306,61353,306,613
nsv5549478RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1253,700,39753,700,397

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058660insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058660Submitted genomicNC_000012.12:g.533
06613_53306614ins1
39
GRCh38 (hg38)NC_000012.12Chr1253,306,61353,306,613
nssv17058660RemappedPerfectNC_000012.11:g.537
00397_53700398ins1
39
GRCh37.p13First PassNC_000012.11Chr1253,700,39753,700,397

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)
nssv17058660<0.00116396
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