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nsv5410373

  • 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: 199 SVs from 39 studies. See in: genome view    
Submitted genomic112,934,687-112,934,738Question Mark
Overlapping variant regions from other studies: 200 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):113,477,309-113,477,360Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5410373Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1112,934,687112,934,738
nsv5410373RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1113,477,309113,477,360

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16908073alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16908073Submitted genomicNC_000001.11:g.112
934687_112934738in
s280
GRCh38 (hg38)NC_000001.11Chr1112,934,687112,934,738
nssv16908073RemappedPerfectNC_000001.10:g.113
477309_113477360in
s280
GRCh37.p13First PassNC_000001.10Chr1113,477,309113,477,360

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)
nssv169080730.003216404
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