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nsv5406131

  • 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 20 studies. See in: genome view    
Submitted genomic32,381,571-32,381,622Question Mark
Overlapping variant regions from other studies: 93 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):32,381,677-32,381,728Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5406131Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr532,381,57132,381,622
nsv5406131RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr532,381,67732,381,728

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16963374alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16963374Submitted genomicNC_000005.10:g.323
81571_32381622ins2
79
GRCh38 (hg38)NC_000005.10Chr532,381,57132,381,622
nssv16963374RemappedPerfectNC_000005.9:g.3238
1677_32381728ins27
9
GRCh37.p13First PassNC_000005.9Chr532,381,67732,381,728

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)
nssv16963374<0.00116404
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