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nsv5543402

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 144 SVs from 22 studies. See in: genome view    
Submitted genomic42,967,586-42,967,588Question Mark
Overlapping variant regions from other studies: 142 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):41,119,603-41,119,605Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5543402Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1742,967,58642,967,588
nsv5543402RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1741,119,60341,119,605

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724546insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724546Submitted genomicNC_000017.11:g.429
67586_42967588ins9
9
GRCh38 (hg38)NC_000017.11Chr1742,967,58642,967,588
nssv17724546RemappedPerfectNC_000017.10:g.411
19603_41119605ins9
9
GRCh37.p13First PassNC_000017.10Chr1741,119,60341,119,605

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)
nssv177245460.4528856404
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