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nsv5420398

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,336

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 27 studies. See in: genome view    
Submitted genomic154,417,650-154,421,985Question Mark
Overlapping variant regions from other studies: 121 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):154,390,126-154,394,461Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5420398Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1154,417,650154,421,985
nsv5420398RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1154,390,126154,394,461

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890374deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890374Submitted genomicNC_000001.11:g.154
417650_154421985de
l
GRCh38 (hg38)NC_000001.11Chr1154,417,650154,421,985
nssv16890374RemappedPerfectNC_000001.10:g.154
390126_154394461de
l
GRCh37.p13First PassNC_000001.10Chr1154,390,126154,394,461

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)
nssv16890374<0.00116404
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