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nsv5509214

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:873

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 25 studies. See in: genome view    
Submitted genomic53,378,055-53,378,927Question Mark
Overlapping variant regions from other studies: 108 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):53,771,839-53,772,711Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5509214Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1253,378,05553,378,927
nsv5509214RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1253,771,83953,772,711

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058673deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058673Submitted genomicNC_000012.12:g.533
78055_53378927del
GRCh38 (hg38)NC_000012.12Chr1253,378,05553,378,927
nssv17058673RemappedPerfectNC_000012.11:g.537
71839_53772711del
GRCh37.p13First PassNC_000012.11Chr1253,771,83953,772,711

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)
nssv17058673<0.00126404
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