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nsv5414194

  • 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: 135 SVs from 25 studies. See in: genome view    
Submitted genomic3,112,516-3,112,567Question Mark
Overlapping variant regions from other studies: 135 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):3,162,517-3,162,568Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5414194Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr163,112,5163,112,567
nsv5414194RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr163,162,5173,162,568

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17706333alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17706333Submitted genomicNC_000016.10:g.311
2516_3112567ins281
GRCh38 (hg38)NC_000016.10Chr163,112,5163,112,567
nssv17706333RemappedPerfectNC_000016.9:g.3162
517_3162568ins281
GRCh37.p13First PassNC_000016.9Chr163,162,5173,162,568

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)
nssv17706333<0.00116404
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