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nsv5501226

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:144

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 178 SVs from 30 studies. See in: genome view    
Submitted genomic1,823,146-1,823,289Question Mark
Overlapping variant regions from other studies: 178 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):1,932,312-1,932,455Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5501226Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr121,823,1461,823,289
nsv5501226RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr121,932,3121,932,455

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17054829deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17054829Submitted genomicNC_000012.12:g.182
3146_1823289del
GRCh38 (hg38)NC_000012.12Chr121,823,1461,823,289
nssv17054829RemappedPerfectNC_000012.11:g.193
2312_1932455del
GRCh37.p13First PassNC_000012.11Chr121,932,3121,932,455

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)
nssv17054829<0.00116404
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