U.S. flag

An official website of the United States government

nsv5533760

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:61

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 17 studies. See in: genome view    
Submitted genomic55,407,449-55,407,509Question Mark
Overlapping variant regions from other studies: 113 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):53,484,810-53,484,870Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5533760Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1755,407,44955,407,509
nsv5533760RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1753,484,81053,484,870

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724767deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724767Submitted genomicNC_000017.11:g.554
07449_55407509del
GRCh38 (hg38)NC_000017.11Chr1755,407,44955,407,509
nssv17724767RemappedPerfectNC_000017.10:g.534
84810_53484870del
GRCh37.p13First PassNC_000017.10Chr1753,484,81053,484,870

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)
nssv17724767<0.00116404
Support Center