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nsv5523991

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,031

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 118 SVs from 25 studies. See in: genome view    
Submitted genomic52,286,177-52,287,207Question Mark
Overlapping variant regions from other studies: 118 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):52,578,374-52,579,404Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523991Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1552,286,17752,287,207
nsv5523991RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1552,578,37452,579,404

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17702752deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17702752Submitted genomicNC_000015.10:g.522
86177_52287207del
GRCh38 (hg38)NC_000015.10Chr1552,286,17752,287,207
nssv17702752RemappedPerfectNC_000015.9:g.5257
8374_52579404del
GRCh37.p13First PassNC_000015.9Chr1552,578,37452,579,404

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)
nssv177027520.002106404
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