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nsv5496441

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:315

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 106 SVs from 25 studies. See in: genome view    
Submitted genomic56,445,298-56,445,612Question Mark
Overlapping variant regions from other studies: 106 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):56,839,082-56,839,396Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5496441Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1256,445,29856,445,612
nsv5496441RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1256,839,08256,839,396

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17057656deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17057656Submitted genomicNC_000012.12:g.564
45298_56445612del
GRCh38 (hg38)NC_000012.12Chr1256,445,29856,445,612
nssv17057656RemappedPerfectNC_000012.11:g.568
39082_56839396del
GRCh37.p13First PassNC_000012.11Chr1256,839,08256,839,396

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)
nssv17057656<0.00136404
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