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nsv5406687

  • 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: 118 SVs from 31 studies. See in: genome view    
Submitted genomic141,407,505-141,407,556Question Mark
Overlapping variant regions from other studies: 116 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):140,787,072-140,787,123Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5406687Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5141,407,505141,407,556
nsv5406687RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5140,787,072140,787,123

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16975417alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16975417Submitted genomicNC_000005.10:g.141
407505_141407556in
s161
GRCh38 (hg38)NC_000005.10Chr5141,407,505141,407,556
nssv16975417RemappedPerfectNC_000005.9:g.1407
87072_140787123ins
161
GRCh37.p13First PassNC_000005.9Chr5140,787,072140,787,123

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)
nssv169754170.0181136296
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