U.S. flag

An official website of the United States government

nsv5430364

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:331

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 593 SVs from 41 studies. See in: genome view    
Submitted genomic1,434,045-1,434,375Question Mark
Overlapping variant regions from other studies: 593 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):1,369,425-1,369,755Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5430364Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr11,434,0451,434,375
nsv5430364RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr11,369,4251,369,755

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16899600deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16899600Submitted genomicNC_000001.11:g.143
4045_1434375del
GRCh38 (hg38)NC_000001.11Chr11,434,0451,434,375
nssv16899600RemappedPerfectNC_000001.10:g.136
9425_1369755del
GRCh37.p13First PassNC_000001.10Chr11,369,4251,369,755

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)
nssv16899600<0.00116404
Support Center