U.S. flag

An official website of the United States government

nsv5482655

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:363

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 101 SVs from 24 studies. See in: genome view    
Submitted genomic86,956,922-86,957,284Question Mark
Overlapping variant regions from other studies: 101 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):89,571,837-89,572,199Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5482655Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr986,956,92286,957,284
nsv5482655RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr989,571,83789,572,199

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17025420deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17025420Submitted genomicNC_000009.12:g.869
56922_86957284del
GRCh38 (hg38)NC_000009.12Chr986,956,92286,957,284
nssv17025420RemappedPerfectNC_000009.11:g.895
71837_89572199del
GRCh37.p13First PassNC_000009.11Chr989,571,83789,572,199

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)
nssv17025420<0.00116404
Support Center