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nsv5508839

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:68,438

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 760 SVs from 81 studies. See in: genome view    
Submitted genomic43,596,437-43,664,874Question Mark
Overlapping variant regions from other studies: 760 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):43,888,635-43,957,072Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5508839Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1543,596,43743,664,874
nsv5508839RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1543,888,63543,957,072

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17702944deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17702944Submitted genomicNC_000015.10:g.435
96437_43664874del
GRCh38 (hg38)NC_000015.10Chr1543,596,43743,664,874
nssv17702944RemappedPerfectNC_000015.9:g.4388
8635_43957072del
GRCh37.p13First PassNC_000015.9Chr1543,888,63543,957,072

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)
nssv177029440.013856402
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