U.S. flag

An official website of the United States government

nsv4578112

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 452 SVs from 11 studies. See in: genome view    
Remapped(Score: Perfect):7,977,741-7,977,741Question Mark
Overlapping variant regions from other studies: 453 SVs from 11 studies. See in: genome view    
Submitted genomic7,945,782-7,945,782Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578112RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX7,977,7417,977,741
nsv4578112Submitted genomicGRCh37.p13Primary AssemblyNC_000023.10ChrX7,945,7827,945,782

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16088895alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16088895RemappedPerfectNC_000023.11:g.797
7741_7977742ins279
GRCh38.p12First PassNC_000023.11ChrX7,977,7417,977,741
nssv16088895Submitted genomicNC_000023.10:g.794
5782_7945783ins279
GRCh37.p13NC_000023.10ChrX7,945,7827,945,782

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)
nssv160888954.6e-005121648
Support Center