U.S. flag

An official website of the United States government

nsv5419333

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 100 SVs from 25 studies. See in: genome view    
Submitted genomic53,338,041-53,338,092Question Mark
Overlapping variant regions from other studies: 100 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):53,731,825-53,731,876Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5419333Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1253,338,04153,338,092
nsv5419333RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1253,731,82553,731,876

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058663alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058663Submitted genomicNC_000012.12:g.533
38041_53338092ins2
79
GRCh38 (hg38)NC_000012.12Chr1253,338,04153,338,092
nssv17058663RemappedPerfectNC_000012.11:g.537
31825_53731876ins2
79
GRCh37.p13First PassNC_000012.11Chr1253,731,82553,731,876

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)
nssv17058663<0.00126404
Support Center