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nsv5422745

  • 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: 81 SVs from 14 studies. See in: genome view    
Submitted genomic32,145,598-32,145,649Question Mark
Overlapping variant regions from other studies: 81 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):30,733,401-30,733,452Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5422745Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2032,145,59832,145,649
nsv5422745RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2030,733,40130,733,452

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17731937alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17731937Submitted genomicNC_000020.11:g.321
45598_32145649ins2
80
GRCh38 (hg38)NC_000020.11Chr2032,145,59832,145,649
nssv17731937RemappedPerfectNC_000020.10:g.307
33401_30733452ins2
80
GRCh37.p13First PassNC_000020.10Chr2030,733,40130,733,452

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)
nssv17731937<0.00116404
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