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nsv5554108

  • 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: 84 SVs from 20 studies. See in: genome view    
Submitted genomic73,943,384-73,943,435Question Mark
Overlapping variant regions from other studies: 84 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):74,410,087-74,410,138Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5554108Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1473,943,38473,943,435
nsv5554108RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1474,410,08774,410,138

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17699253line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17699253Submitted genomicNC_000014.9:g.7394
3384_73943435ins36
8
GRCh38 (hg38)NC_000014.9Chr1473,943,38473,943,435
nssv17699253RemappedPerfectNC_000014.8:g.7441
0087_74410138ins36
8
GRCh37.p13First PassNC_000014.8Chr1474,410,08774,410,138

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)
nssv17699253<0.00116404
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