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nsv5523178

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,635

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 311 SVs from 51 studies. See in: genome view    
Submitted genomic41,055,245-41,065,879Question Mark
Overlapping variant regions from other studies: 309 SVs from 51 studies. See in: genome view    
Remapped(Score: Perfect):39,211,497-39,222,131Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523178Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1741,055,24541,065,879
nsv5523178RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1739,211,49739,222,131

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713151deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713151Submitted genomicNC_000017.11:g.410
55245_41065879del
GRCh38 (hg38)NC_000017.11Chr1741,055,24541,065,879
nssv17713151RemappedPerfectNC_000017.10:g.392
11497_39222131del
GRCh37.p13First PassNC_000017.10Chr1739,211,49739,222,131

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)
nssv177131510.007426404
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