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nsv5430689

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,466

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 767 SVs from 60 studies. See in: genome view    
Submitted genomic1,738,203-1,740,668Question Mark
Overlapping variant regions from other studies: 767 SVs from 60 studies. See in: genome view    
Remapped(Score: Perfect):1,669,642-1,672,107Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5430689Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr11,738,2031,740,668
nsv5430689RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr11,669,6421,672,107

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16902515deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16902515Submitted genomicNC_000001.11:g.173
8203_1740668del
GRCh38 (hg38)NC_000001.11Chr11,738,2031,740,668
nssv16902515RemappedPerfectNC_000001.10:g.166
9642_1672107del
GRCh37.p13First PassNC_000001.10Chr11,669,6421,672,107

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)
nssv16902515<0.00136404
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