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nsv5406492

  • 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: 93 SVs from 19 studies. See in: genome view    
Submitted genomic70,286,436-70,286,487Question Mark
Overlapping variant regions from other studies: 92 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):70,513,568-70,513,619Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5406492Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr270,286,43670,286,487
nsv5406492RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr270,513,56870,513,619

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16914448alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16914448Submitted genomicNC_000002.12:g.702
86436_70286487ins2
78
GRCh38 (hg38)NC_000002.12Chr270,286,43670,286,487
nssv16914448RemappedPerfectNC_000002.11:g.705
13568_70513619ins2
78
GRCh37.p13First PassNC_000002.11Chr270,513,56870,513,619

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)
nssv169144480.006406404
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