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nsv5469450

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:827

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 84 SVs from 25 studies. See in: genome view    
Submitted genomic42,358,440-42,359,266Question Mark
Overlapping variant regions from other studies: 84 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):42,360,457-42,361,283Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5469450Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr442,358,44042,359,266
nsv5469450RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr442,360,45742,361,283

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16949642deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16949642Submitted genomicNC_000004.12:g.423
58440_42359266del
GRCh38 (hg38)NC_000004.12Chr442,358,44042,359,266
nssv16949642RemappedPerfectNC_000004.11:g.423
60457_42361283del
GRCh37.p13First PassNC_000004.11Chr442,360,45742,361,283

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)
nssv16949642<0.00136404
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