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nsv5509187

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,896

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 38 studies. See in: genome view    
Submitted genomic50,418,076-50,423,971Question Mark
Overlapping variant regions from other studies: 113 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):50,811,859-50,817,754Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5509187Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1250,418,07650,423,971
nsv5509187RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1250,811,85950,817,754

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17056489deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17056489Submitted genomicNC_000012.12:g.504
18076_50423971del
GRCh38 (hg38)NC_000012.12Chr1250,418,07650,423,971
nssv17056489RemappedPerfectNC_000012.11:g.508
11859_50817754del
GRCh37.p13First PassNC_000012.11Chr1250,811,85950,817,754

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)
nssv17056489<0.00116404
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