U.S. flag

An official website of the United States government

nsv5480919

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:333

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 50 studies. See in: genome view    
Submitted genomic91,209,474-91,209,806Question Mark
Overlapping variant regions from other studies: 121 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):92,969,231-92,969,563Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5480919Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1091,209,47491,209,806
nsv5480919RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1092,969,23192,969,563

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17036875deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17036875Submitted genomicNC_000010.11:g.912
09474_91209806del
GRCh38 (hg38)NC_000010.11Chr1091,209,47491,209,806
nssv17036875RemappedPerfectNC_000010.10:g.929
69231_92969563del
GRCh37.p13First PassNC_000010.10Chr1092,969,23192,969,563

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)
nssv170368750.89557346404
Support Center