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nsv5397100

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 110 SVs from 26 studies. See in: genome view    
Submitted genomic115,321,874-115,321,915Question Mark
Overlapping variant regions from other studies: 112 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):115,864,495-115,864,536Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5397100Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1115,321,874115,321,915
nsv5397100RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1115,864,495115,864,536

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16889308alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16889308Submitted genomicNC_000001.11:g.115
321874_115321915in
s313
GRCh38 (hg38)NC_000001.11Chr1115,321,874115,321,915
nssv16889308RemappedPerfectNC_000001.10:g.115
864495_115864536in
s313
GRCh37.p13First PassNC_000001.10Chr1115,864,495115,864,536

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)
nssv16889308<0.00126404
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