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nsv5439590

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:66

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 82 SVs from 19 studies. See in: genome view    
Submitted genomic44,872,653-44,872,718Question Mark
Overlapping variant regions from other studies: 82 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):44,914,145-44,914,210Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5439590Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr344,872,65344,872,718
nsv5439590RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr344,914,14544,914,210

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933668duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933668Submitted genomicNC_000003.12:g.448
72653_44872718dup
GRCh38 (hg38)NC_000003.12Chr344,872,65344,872,718
nssv16933668RemappedPerfectNC_000003.11:g.449
14145_44914210dup
GRCh37.p13First PassNC_000003.11Chr344,914,14544,914,210

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)
nssv16933668<0.00126404
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