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nsv5482290

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:89,328

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 289 SVs from 49 studies. See in: genome view    
Submitted genomic50,485,836-50,575,163Question Mark
Overlapping variant regions from other studies: 289 SVs from 49 studies. See in: genome view    
Remapped(Score: Good):50,553,534-50,642,860Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5482290Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr750,485,83650,575,163
nsv5482290RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr750,553,53450,642,860

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16995674duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16995674Submitted genomicNC_000007.14:g.504
85836_50575163dup
GRCh38 (hg38)NC_000007.14Chr750,485,83650,575,163
nssv16995674RemappedGoodNC_000007.13:g.505
53534_50642860dup
GRCh37.p13First PassNC_000007.13Chr750,553,53450,642,860

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)
nssv16995674<0.00116404
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