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nsv5324004

  • 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: 115 SVs from 22 studies. See in: genome view    
Submitted genomic127,176,550-127,176,550Question Mark
Overlapping variant regions from other studies: 114 SVs from 22 studies. See in: genome view    
Submitted genomic127,176,619-127,176,619Question Mark
Overlapping variant regions from other studies: 115 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):127,497,695-127,497,695Question Mark
Overlapping variant regions from other studies: 114 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):127,497,764-127,497,764Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv5324004Submitted genomicGRCh38.p13Primary AssemblyNC_000006.12Chr6127,176,550127,176,550+
nsv5324004Submitted genomicGRCh38.p13Primary AssemblyNC_000006.12Chr6127,176,619127,176,619+
nsv5324004RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6127,497,695127,497,695+
nsv5324004RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6127,497,764127,497,764+

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16776682intrachromosomal translocationSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv16776682Submitted genomicGRCh38.p13NC_000006.12Chr6127,176,550127,176,550+
nssv16776682Submitted genomicGRCh38.p13NC_000006.12Chr6127,176,619127,176,619+
nssv16776682RemappedPerfectGRCh37.p13First PassNC_000006.11Chr6127,497,695127,497,695+
nssv16776682RemappedPerfectGRCh37.p13First PassNC_000006.11Chr6127,497,764127,497,764+

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)
nssv16776682<0.001
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