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nsv5495511

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:972

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 161 SVs from 20 studies. See in: genome view    
Submitted genomic51,002,588-51,003,559Question Mark
Overlapping variant regions from other studies: 161 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):51,576,724-51,577,695Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5495511Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1351,002,58851,003,559
nsv5495511RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1351,576,72451,577,695

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17687731deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17687731Submitted genomicNC_000013.11:g.510
02588_51003559del
GRCh38 (hg38)NC_000013.11Chr1351,002,58851,003,559
nssv17687731RemappedPerfectNC_000013.10:g.515
76724_51577695del
GRCh37.p13First PassNC_000013.10Chr1351,576,72451,577,695

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)
nssv17687731<0.00116404
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