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nsv5519628

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:302

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 132 SVs from 15 studies. See in: genome view    
Submitted genomic48,890,775-48,891,076Question Mark
Overlapping variant regions from other studies: 130 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):46,968,137-46,968,438Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5519628Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1748,890,77548,891,076
nsv5519628RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1746,968,13746,968,438

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724609deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724609Submitted genomicNC_000017.11:g.488
90775_48891076del
GRCh38 (hg38)NC_000017.11Chr1748,890,77548,891,076
nssv17724609RemappedPerfectNC_000017.10:g.469
68137_46968438del
GRCh37.p13First PassNC_000017.10Chr1746,968,13746,968,438

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)
nssv17724609<0.00126404
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