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nsv5459544

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:144

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 120 SVs from 20 studies. See in: genome view    
Submitted genomic90,277,080-90,277,223Question Mark
Overlapping variant regions from other studies: 120 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):89,572,897-89,573,040Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5459544Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr590,277,08090,277,223
nsv5459544RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr589,572,89789,573,040

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16971321duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16971321Submitted genomicNC_000005.10:g.902
77080_90277223dup
GRCh38 (hg38)NC_000005.10Chr590,277,08090,277,223
nssv16971321RemappedPerfectNC_000005.9:g.8957
2897_89573040dup
GRCh37.p13First PassNC_000005.9Chr589,572,89789,573,040

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)
nssv16971321<0.00116404
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