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nsv5417299

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,690

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 159 SVs from 40 studies. See in: genome view    
Submitted genomic30,006,936-30,016,625Question Mark
Overlapping variant regions from other studies: 159 SVs from 40 studies. See in: genome view    
Remapped(Score: Perfect):30,479,783-30,489,472Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5417299Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr130,006,93630,016,625
nsv5417299RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr130,479,78330,489,472

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16903529deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16903529Submitted genomicNC_000001.11:g.300
06936_30016625del
GRCh38 (hg38)NC_000001.11Chr130,006,93630,016,625
nssv16903529RemappedPerfectNC_000001.10:g.304
79783_30489472del
GRCh37.p13First PassNC_000001.10Chr130,479,78330,489,472

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)
nssv169035290.004246404
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