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nsv5463772

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:341

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 92 SVs from 13 studies. See in: genome view    
Submitted genomic138,842,417-138,842,757Question Mark
Overlapping variant regions from other studies: 92 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):139,163,554-139,163,894Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5463772Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6138,842,417138,842,757
nsv5463772RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6139,163,554139,163,894

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16970849duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16970849Submitted genomicNC_000006.12:g.138
842417_138842757du
p
GRCh38 (hg38)NC_000006.12Chr6138,842,417138,842,757
nssv16970849RemappedPerfectNC_000006.11:g.139
163554_139163894du
p
GRCh37.p13First PassNC_000006.11Chr6139,163,554139,163,894

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)
nssv16970849<0.00126404
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