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nsv5449623

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:582

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 28 studies. See in: genome view    
Submitted genomic48,667,219-48,667,800Question Mark
Overlapping variant regions from other studies: 97 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):48,704,652-48,705,233Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5449623Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr348,667,21948,667,800
nsv5449623RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr348,704,65248,705,233

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933751duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933751Submitted genomicNC_000003.12:g.486
67219_48667800dup
GRCh38 (hg38)NC_000003.12Chr348,667,21948,667,800
nssv16933751RemappedPerfectNC_000003.11:g.487
04652_48705233dup
GRCh37.p13First PassNC_000003.11Chr348,704,65248,705,233

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)
nssv16933751<0.00136404
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