U.S. flag

An official website of the United States government

nsv5415260

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:78

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 178 SVs from 46 studies. See in: genome view    
Submitted genomic151,366,977-151,367,054Question Mark
Overlapping variant regions from other studies: 191 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):151,339,453-151,339,530Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5415260Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1151,366,977151,367,054
nsv5415260RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1151,339,453151,339,530

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890282duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890282Submitted genomicNC_000001.11:g.151
366977_151367054du
p
GRCh38 (hg38)NC_000001.11Chr1151,366,977151,367,054
nssv16890282RemappedPerfectNC_000001.10:g.151
339453_151339530du
p
GRCh37.p13First PassNC_000001.10Chr1151,339,453151,339,530

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)
nssv16890282<0.00116404
Support Center