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nsv5480574

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:644

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 110 SVs from 19 studies. See in: genome view    
Submitted genomic58,496,598-58,497,241Question Mark
Overlapping variant regions from other studies: 110 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):59,409,157-59,409,800Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5480574Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr858,496,59858,497,241
nsv5480574RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr859,409,15759,409,800

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17012425deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17012425Submitted genomicNC_000008.11:g.584
96598_58497241del
GRCh38 (hg38)NC_000008.11Chr858,496,59858,497,241
nssv17012425RemappedPerfectNC_000008.10:g.594
09157_59409800del
GRCh37.p13First PassNC_000008.10Chr859,409,15759,409,800

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)
nssv17012425<0.00116404
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