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nsv5500686

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:70

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 22 studies. See in: genome view    
Submitted genomic82,889,984-82,890,053Question Mark
Overlapping variant regions from other studies: 94 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):82,601,026-82,601,095Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5500686Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1182,889,98482,890,053
nsv5500686RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1182,601,02682,601,095

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17048406deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17048406Submitted genomicNC_000011.10:g.828
89984_82890053del
GRCh38 (hg38)NC_000011.10Chr1182,889,98482,890,053
nssv17048406RemappedPerfectNC_000011.9:g.8260
1026_82601095del
GRCh37.p13First PassNC_000011.9Chr1182,601,02682,601,095

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)
nssv170484060.002166404
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