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nsv5520740

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,260

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 102 SVs from 20 studies. See in: genome view    
Submitted genomic29,056,852-29,058,111Question Mark
Overlapping variant regions from other studies: 102 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):27,383,870-27,385,129Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5520740Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1729,056,85229,058,111
nsv5520740RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1727,383,87027,385,129

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17712398deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17712398Submitted genomicNC_000017.11:g.290
56852_29058111del
GRCh38 (hg38)NC_000017.11Chr1729,056,85229,058,111
nssv17712398RemappedPerfectNC_000017.10:g.273
83870_27385129del
GRCh37.p13First PassNC_000017.10Chr1727,383,87027,385,129

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)
nssv17712398<0.00116404
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