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nsv5505693

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:299

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 25 studies. See in: genome view    
Submitted genomic82,882,496-82,882,794Question Mark
Overlapping variant regions from other studies: 99 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):82,593,538-82,593,836Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5505693Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1182,882,49682,882,794
nsv5505693RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1182,593,53882,593,836

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17048403deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17048403Submitted genomicNC_000011.10:g.828
82496_82882794del
GRCh38 (hg38)NC_000011.10Chr1182,882,49682,882,794
nssv17048403RemappedPerfectNC_000011.9:g.8259
3538_82593836del
GRCh37.p13First PassNC_000011.9Chr1182,593,53882,593,836

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)
nssv170484030.0171076404
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