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nsv5514291

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,664

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 313 SVs from 60 studies. See in: genome view    
Submitted genomic37,418,621-37,422,284Question Mark
Overlapping variant regions from other studies: 363 SVs from 61 studies. See in: genome view    
Remapped(Score: Good):35,778,706-35,782,390Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514291Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1737,418,62137,422,284
nsv5514291RemappedGoodGRCh37.p13Primary AssemblySecond PassNC_000017.10Chr1735,778,70635,782,390

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17712906deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17712906Submitted genomicNC_000017.11:g.374
18621_37422284del
GRCh38 (hg38)NC_000017.11Chr1737,418,62137,422,284
nssv17712906RemappedGoodNC_000017.10:g.357
78706_35782390del
GRCh37.p13Second PassNC_000017.10Chr1735,778,70635,782,390

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)
nssv177129060.1298286404
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