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nsv5474240

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,384

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 133 SVs from 39 studies. See in: genome view    
Submitted genomic86,666,359-86,676,742Question Mark
Overlapping variant regions from other studies: 133 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):86,295,675-86,306,058Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5474240Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr786,666,35986,676,742
nsv5474240RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr786,295,67586,306,058

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16999537deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16999537Submitted genomicNC_000007.14:g.866
66359_86676742del
GRCh38 (hg38)NC_000007.14Chr786,666,35986,676,742
nssv16999537RemappedPerfectNC_000007.13:g.862
95675_86306058del
GRCh37.p13First PassNC_000007.13Chr786,295,67586,306,058

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)
nssv16999537<0.00116404
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