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nsv5484862

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,674

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 185 SVs from 40 studies. See in: genome view    
Submitted genomic39,336,998-39,340,671Question Mark
Overlapping variant regions from other studies: 185 SVs from 40 studies. See in: genome view    
Remapped(Score: Perfect):39,194,517-39,198,190Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5484862Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr839,336,99839,340,671
nsv5484862RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr839,194,51739,198,190

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17009593deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17009593Submitted genomicNC_000008.11:g.393
36998_39340671del
GRCh38 (hg38)NC_000008.11Chr839,336,99839,340,671
nssv17009593RemappedPerfectNC_000008.10:g.391
94517_39198190del
GRCh37.p13First PassNC_000008.10Chr839,194,51739,198,190

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)
nssv17009593<0.00116404
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