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nsv5559867

  • 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: 110 SVs from 26 studies. See in: genome view    
Submitted genomic56,279,356-56,279,407Question Mark
Overlapping variant regions from other studies: 110 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):56,673,140-56,673,191Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5559867Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1256,279,35656,279,407
nsv5559867RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1256,673,14056,673,191

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17057631sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17057631Submitted genomicNC_000012.12:g.562
79356_56279407ins3
37
GRCh38 (hg38)NC_000012.12Chr1256,279,35656,279,407
nssv17057631RemappedPerfectNC_000012.11:g.566
73140_56673191ins3
37
GRCh37.p13First PassNC_000012.11Chr1256,673,14056,673,191

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)
nssv17057631<0.00126402
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