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nsv5531581

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,507

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 222 SVs from 19 studies. See in: genome view    
Submitted genomic12,715,152-12,716,658Question Mark
Overlapping variant regions from other studies: 222 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):12,715,151-12,716,657Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5531581Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1812,715,15212,716,658
nsv5531581RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1812,715,15112,716,657

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17716328deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17716328Submitted genomicNC_000018.10:g.127
15152_12716658del
GRCh38 (hg38)NC_000018.10Chr1812,715,15212,716,658
nssv17716328RemappedPerfectNC_000018.9:g.1271
5151_12716657del
GRCh37.p13First PassNC_000018.9Chr1812,715,15112,716,657

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)
nssv17716328<0.00116404
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