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nsv5528459

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:239,579

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 913 SVs from 76 studies. See in: genome view    
Submitted genomic36,632,408-36,871,986Question Mark
Overlapping variant regions from other studies: 913 SVs from 76 studies. See in: genome view    
Remapped(Score: Perfect):37,123,310-37,362,888Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528459Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,632,40836,871,986
nsv5528459RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1937,123,31037,362,888

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723118deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723118Submitted genomicNC_000019.10:g.366
32408_36871986del
GRCh38 (hg38)NC_000019.10Chr1936,632,40836,871,986
nssv17723118RemappedPerfectNC_000019.9:g.3712
3310_37362888del
GRCh37.p13First PassNC_000019.9Chr1937,123,31037,362,888

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)
nssv17723118<0.00116404
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