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nsv5509859

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,683

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 27 studies. See in: genome view    
Submitted genomic56,226,738-56,228,420Question Mark
Overlapping variant regions from other studies: 114 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):56,620,522-56,622,204Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5509859Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1256,226,73856,228,420
nsv5509859RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1256,620,52256,622,204

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17057627deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17057627Submitted genomicNC_000012.12:g.562
26738_56228420del
GRCh38 (hg38)NC_000012.12Chr1256,226,73856,228,420
nssv17057627RemappedPerfectNC_000012.11:g.566
20522_56622204del
GRCh37.p13First PassNC_000012.11Chr1256,620,52256,622,204

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)
nssv17057627<0.00116404
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