U.S. flag

An official website of the United States government

nsv5562484

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 109 SVs from 30 studies. See in: genome view    
Submitted genomic93,906,947-93,907,020Question Mark
Overlapping variant regions from other studies: 109 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):93,536,259-93,536,332Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5562484Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr793,906,94793,907,020
nsv5562484RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr793,536,25993,536,332

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17000382inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17000382Submitted genomicNC_000007.14:g.939
06947_93907020inv
GRCh38 (hg38)NC_000007.14Chr793,906,94793,907,020
nssv17000382RemappedPerfectNC_000007.13:g.935
36259_93536332inv
GRCh37.p13First PassNC_000007.13Chr793,536,25993,536,332

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)
nssv170003820.0523366404
Support Center