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nsv5415322

  • 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: 86 SVs from 17 studies. See in: genome view    
Submitted genomic57,400,732-57,400,783Question Mark
Overlapping variant regions from other studies: 86 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):57,867,450-57,867,501Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5415322Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1457,400,73257,400,783
nsv5415322RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1457,867,45057,867,501

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17694898alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17694898Submitted genomicNC_000014.9:g.5740
0732_57400783ins28
1
GRCh38 (hg38)NC_000014.9Chr1457,400,73257,400,783
nssv17694898RemappedPerfectNC_000014.8:g.5786
7450_57867501ins28
1
GRCh37.p13First PassNC_000014.8Chr1457,867,45057,867,501

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)
nssv17694898<0.00116404
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