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nsv5323121

  • 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: 120 SVs from 20 studies. See in: genome view    
Submitted genomic36,118,613-36,118,613Question Mark
Overlapping variant regions from other studies: 120 SVs from 20 studies. See in: genome view    
Submitted genomic36,118,731-36,118,731Question Mark
Overlapping variant regions from other studies: 120 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):36,609,515-36,609,515Question Mark
Overlapping variant regions from other studies: 120 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):36,609,633-36,609,633Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv5323121Submitted genomicGRCh38.p13Primary AssemblyNC_000019.10Chr1936,118,61336,118,613+
nsv5323121Submitted genomicGRCh38.p13Primary AssemblyNC_000019.10Chr1936,118,73136,118,731+
nsv5323121RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,609,51536,609,515+
nsv5323121RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,609,63336,609,633+

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16763174intrachromosomal translocationSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv16763174Submitted genomicGRCh38.p13NC_000019.10Chr1936,118,61336,118,613+
nssv16763174Submitted genomicGRCh38.p13NC_000019.10Chr1936,118,73136,118,731+
nssv16763174RemappedPerfectGRCh37.p13First PassNC_000019.9Chr1936,609,51536,609,515+
nssv16763174RemappedPerfectGRCh37.p13First PassNC_000019.9Chr1936,609,63336,609,633+

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)
nssv16763174<0.001
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