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nsv5547390

  • 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: 137 SVs from 18 studies. See in: genome view    
Submitted genomic43,031,256-43,031,256Question Mark
Overlapping variant regions from other studies: 135 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):41,183,273-41,183,273Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5547390Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1743,031,25643,031,256
nsv5547390RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1741,183,27341,183,273

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724554insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724554Submitted genomicNC_000017.11:g.430
31256_43031257ins2
97
GRCh38 (hg38)NC_000017.11Chr1743,031,25643,031,256
nssv17724554RemappedPerfectNC_000017.10:g.411
83273_41183274ins2
97
GRCh37.p13First PassNC_000017.10Chr1741,183,27341,183,273

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)
nssv17724554<0.00126386
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