U.S. flag

An official website of the United States government

nsv5519239

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,704

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 153 SVs from 22 studies. See in: genome view    
Submitted genomic60,475,155-60,478,858Question Mark
Overlapping variant regions from other studies: 153 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):58,552,516-58,556,219Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5519239Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1760,475,15560,478,858
nsv5519239RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1758,552,51658,556,219

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724893duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724893Submitted genomicNC_000017.11:g.604
75155_60478858dup
GRCh38 (hg38)NC_000017.11Chr1760,475,15560,478,858
nssv17724893RemappedPerfectNC_000017.10:g.585
52516_58556219dup
GRCh37.p13First PassNC_000017.10Chr1758,552,51658,556,219

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)
nssv17724893<0.00116404
Support Center