nsv5379391

  • 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: 198 SVs from 17 studies. See in: genome view    
Submitted genomic123,503,233-123,503,233Question Mark
Overlapping variant regions from other studies: 198 SVs from 17 studies. See in: genome view    
Submitted genomic123,507,514-123,507,514Question Mark
Overlapping variant regions from other studies: 198 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):124,515,473-124,515,473Question Mark
Overlapping variant regions from other studies: 198 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):124,519,754-124,519,754Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv5379391Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8123,503,233123,503,233+
nsv5379391Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8123,507,514123,507,514+
nsv5379391RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8124,515,473124,515,473+
nsv5379391RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8124,519,754124,519,754+

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16506618intrachromosomal translocationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv16506618Submitted genomicGRCh38 (hg38)NC_000008.11Chr8123,503,233123,503,233+
nssv16506618Submitted genomicGRCh38 (hg38)NC_000008.11Chr8123,507,514123,507,514+
nssv16506618RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8124,515,473124,515,473+
nssv16506618RemappedPerfectGRCh37.p13First PassNC_000008.10Chr8124,519,754124,519,754+

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)
nssv16506618<0.001129246
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