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nsv5452518

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:433

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 126 SVs from 31 studies. See in: genome view    
Submitted genomic127,810,847-127,811,279Question Mark
Overlapping variant regions from other studies: 126 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):127,529,690-127,530,122Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5452518Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3127,810,847127,811,279
nsv5452518RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3127,529,690127,530,122

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16939578deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16939578Submitted genomicNC_000003.12:g.127
810847_127811279de
l
GRCh38 (hg38)NC_000003.12Chr3127,810,847127,811,279
nssv16939578RemappedPerfectNC_000003.11:g.127
529690_127530122de
l
GRCh37.p13First PassNC_000003.11Chr3127,529,690127,530,122

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)
nssv169395780.0714556404
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