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nsv5514282

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:59

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 154 SVs from 30 studies. See in: genome view    
Submitted genomic89,630,835-89,630,893Question Mark
Overlapping variant regions from other studies: 154 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):90,174,066-90,174,124Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514282Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1589,630,83589,630,893
nsv5514282RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1590,174,06690,174,124

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17704133deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17704133Submitted genomicNC_000015.10:g.896
30835_89630893del
GRCh38 (hg38)NC_000015.10Chr1589,630,83589,630,893
nssv17704133RemappedPerfectNC_000015.9:g.9017
4066_90174124del
GRCh37.p13First PassNC_000015.9Chr1590,174,06690,174,124

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)
nssv17704133<0.00156404
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