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nsv5512671

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,393

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 175 SVs from 31 studies. See in: genome view    
Submitted genomic5,226,163-5,227,555Question Mark
Overlapping variant regions from other studies: 175 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):5,247,393-5,248,785Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5512671Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr115,226,1635,227,555
nsv5512671RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr115,247,3935,248,785

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17041693deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17041693Submitted genomicNC_000011.10:g.522
6163_5227555del
GRCh38 (hg38)NC_000011.10Chr115,226,1635,227,555
nssv17041693RemappedPerfectNC_000011.9:g.5247
393_5248785del
GRCh37.p13First PassNC_000011.9Chr115,247,3935,248,785

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)
nssv17041693<0.00126404
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