U.S. flag

An official website of the United States government

nsv5365219

  • 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: 82 SVs from 26 studies. See in: genome view    
Submitted genomic110,475,058-110,475,058Question Mark
Overlapping variant regions from other studies: 191 SVs from 33 studies. See in: genome view    
Submitted genomic21,153,595-21,153,595Question Mark
Overlapping variant regions from other studies: 82 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):110,912,863-110,912,863Question Mark
Overlapping variant regions from other studies: 191 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):21,727,734-21,727,734Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv5365219Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12110,475,058110,475,058+
nsv5365219Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1321,153,59521,153,595+
nsv5365219RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12110,912,863110,912,863+
nsv5365219RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1321,727,73421,727,734+

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16553140interchromosomal translocationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv16553140Submitted genomicGRCh38 (hg38)NC_000012.12Chr12110,475,058110,475,058+
nssv16553140Submitted genomicGRCh38 (hg38)NC_000013.11Chr1321,153,59521,153,595+
nssv16553140RemappedPerfectGRCh37.p13First PassNC_000012.11Chr12110,912,863110,912,863+
nssv16553140RemappedPerfectGRCh37.p13First PassNC_000013.10Chr1321,727,73421,727,734+

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16553140<0.001229246
Support Center