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nsv5496032

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:105

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 100 SVs from 24 studies. See in: genome view    
Submitted genomic53,331,649-53,331,753Question Mark
Overlapping variant regions from other studies: 100 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):53,725,433-53,725,537Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5496032Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1253,331,64953,331,753
nsv5496032RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1253,725,43353,725,537

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058662deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058662Submitted genomicNC_000012.12:g.533
31649_53331753del
GRCh38 (hg38)NC_000012.12Chr1253,331,64953,331,753
nssv17058662RemappedPerfectNC_000012.11:g.537
25433_53725537del
GRCh37.p13First PassNC_000012.11Chr1253,725,43353,725,537

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)
nssv17058662<0.00136404
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