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nsv5496880

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,534

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 84 SVs from 17 studies. See in: genome view    
Submitted genomic82,851,464-82,852,997Question Mark
Overlapping variant regions from other studies: 84 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):82,562,506-82,564,039Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5496880Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1182,851,46482,852,997
nsv5496880RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1182,562,50682,564,039

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17048091deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17048091Submitted genomicNC_000011.10:g.828
51464_82852997del
GRCh38 (hg38)NC_000011.10Chr1182,851,46482,852,997
nssv17048091RemappedPerfectNC_000011.9:g.8256
2506_82564039del
GRCh37.p13First PassNC_000011.9Chr1182,562,50682,564,039

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)
nssv17048091<0.00116404
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