U.S. flag

An official website of the United States government

nsv5486036

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:453

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 153 SVs from 33 studies. See in: genome view    
Submitted genomic80,482,369-80,482,821Question Mark
Overlapping variant regions from other studies: 153 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):82,242,125-82,242,577Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5486036Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1080,482,36980,482,821
nsv5486036RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1082,242,12582,242,577

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17037133deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17037133Submitted genomicNC_000010.11:g.804
82369_80482821del
GRCh38 (hg38)NC_000010.11Chr1080,482,36980,482,821
nssv17037133RemappedPerfectNC_000010.10:g.822
42125_82242577del
GRCh37.p13First PassNC_000010.10Chr1082,242,12582,242,577

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)
nssv170371330.0231486352
Support Center