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nsv5507414

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:61

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 135 SVs from 27 studies. See in: genome view    
Submitted genomic12,874,339-12,874,399Question Mark
Overlapping variant regions from other studies: 136 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):13,027,273-13,027,333Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5507414Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1212,874,33912,874,399
nsv5507414RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1213,027,27313,027,333

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17053237deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17053237Submitted genomicNC_000012.12:g.128
74339_12874399del
GRCh38 (hg38)NC_000012.12Chr1212,874,33912,874,399
nssv17053237RemappedPerfectNC_000012.11:g.130
27273_13027333del
GRCh37.p13First PassNC_000012.11Chr1213,027,27313,027,333

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)
nssv17053237<0.00146404
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