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nsv5418392

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 22 studies. See in: genome view    
Submitted genomic40,566,819-40,566,870Question Mark
Overlapping variant regions from other studies: 121 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):41,140,956-41,141,007Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5418392Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1340,566,81940,566,870
nsv5418392RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1341,140,95641,141,007

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17687095alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17687095Submitted genomicNC_000013.11:g.405
66819_40566870ins2
81
GRCh38 (hg38)NC_000013.11Chr1340,566,81940,566,870
nssv17687095RemappedPerfectNC_000013.10:g.411
40956_41141007ins2
81
GRCh37.p13First PassNC_000013.10Chr1341,140,95641,141,007

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)
nssv17687095<0.00126404
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