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nsv5408378

  • 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: 100 SVs from 23 studies. See in: genome view    
Submitted genomic63,873,180-63,873,231Question Mark
Overlapping variant regions from other studies: 100 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):63,858,856-63,858,907Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5408378Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr363,873,18063,873,231
nsv5408378RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr363,858,85663,858,907

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933896alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933896Submitted genomicNC_000003.12:g.638
73180_63873231ins2
80
GRCh38 (hg38)NC_000003.12Chr363,873,18063,873,231
nssv16933896RemappedPerfectNC_000003.11:g.638
58856_63858907ins2
80
GRCh37.p13First PassNC_000003.11Chr363,858,85663,858,907

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)
nssv16933896<0.00136404
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