U.S. flag

An official website of the United States government

nsv5410185

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 137 SVs from 34 studies. See in: genome view    
Submitted genomic50,199,278-50,199,329Question Mark
Overlapping variant regions from other studies: 140 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):51,959,038-51,959,089Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5410185Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1050,199,27850,199,329
nsv5410185RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1051,959,03851,959,089

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17034679alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17034679Submitted genomicNC_000010.11:g.501
99278_50199329ins2
81
GRCh38 (hg38)NC_000010.11Chr1050,199,27850,199,329
nssv17034679RemappedPerfectNC_000010.10:g.519
59038_51959089ins2
81
GRCh37.p13First PassNC_000010.10Chr1051,959,03851,959,089

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)
nssv17034679<0.00116404
Support Center