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nsv5470770

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,477

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 96 SVs from 19 studies. See in: genome view    
Submitted genomic133,894,739-133,896,215Question Mark
Overlapping variant regions from other studies: 96 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):134,215,877-134,217,353Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5470770Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6133,894,739133,896,215
nsv5470770RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6134,215,877134,217,353

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16969783deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16969783Submitted genomicNC_000006.12:g.133
894739_133896215de
l
GRCh38 (hg38)NC_000006.12Chr6133,894,739133,896,215
nssv16969783RemappedPerfectNC_000006.11:g.134
215877_134217353de
l
GRCh37.p13First PassNC_000006.11Chr6134,215,877134,217,353

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)
nssv16969783<0.00116404
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