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nsv5405136

  • 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 21 studies. See in: genome view    
Submitted genomic90,286,226-90,286,277Question Mark
Overlapping variant regions from other studies: 121 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):89,582,043-89,582,094Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5405136Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr590,286,22690,286,277
nsv5405136RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr589,582,04389,582,094

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16971322alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16971322Submitted genomicNC_000005.10:g.902
86226_90286277ins1
29
GRCh38 (hg38)NC_000005.10Chr590,286,22690,286,277
nssv16971322RemappedPerfectNC_000005.9:g.8958
2043_89582094ins12
9
GRCh37.p13First PassNC_000005.9Chr589,582,04389,582,094

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)
nssv16971322<0.00126404
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