U.S. flag

An official website of the United States government

nsv5492503

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:294,876

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 962 SVs from 81 studies. See in: genome view    
Submitted genomic55,675,309-55,970,184Question Mark
Overlapping variant regions from other studies: 962 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):57,435,069-57,729,944Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5492503Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1055,675,30955,970,184
nsv5492503RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1057,435,06957,729,944

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17034277deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17034277Submitted genomicNC_000010.11:g.556
75309_55970184del
GRCh38 (hg38)NC_000010.11Chr1055,675,30955,970,184
nssv17034277RemappedPerfectNC_000010.10:g.574
35069_57729944del
GRCh37.p13First PassNC_000010.10Chr1057,435,06957,729,944

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)
nssv17034277<0.00126404
Support Center