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nsv5514507

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:855

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 35 studies. See in: genome view    
Submitted genomic4,737,312-4,738,166Question Mark
Overlapping variant regions from other studies: 136 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):4,640,607-4,641,461Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514507Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr174,737,3124,738,166
nsv5514507RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr174,640,6074,641,461

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17711002deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17711002Submitted genomicNC_000017.11:g.473
7312_4738166del
GRCh38 (hg38)NC_000017.11Chr174,737,3124,738,166
nssv17711002RemappedPerfectNC_000017.10:g.464
0607_4641461del
GRCh37.p13First PassNC_000017.10Chr174,640,6074,641,461

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)
nssv177110020.0311996404
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