U.S. flag

An official website of the United States government

nsv5423230

  • 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: 112 SVs from 17 studies. See in: genome view    
Submitted genomic65,048,331-65,048,382Question Mark
Overlapping variant regions from other studies: 112 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):63,044,449-63,044,500Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1765,048,33165,048,382
nsv5423230RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1763,044,44963,044,500

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714107alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714107Submitted genomicNC_000017.11:g.650
48331_65048382ins2
65
GRCh38 (hg38)NC_000017.11Chr1765,048,33165,048,382
nssv17714107RemappedPerfectNC_000017.10:g.630
44449_63044500ins2
65
GRCh37.p13First PassNC_000017.10Chr1763,044,44963,044,500

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)
nssv177141070.004286404
Support Center