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nsv5522286

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,535

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 153 SVs from 24 studies. See in: genome view    
Submitted genomic48,080,685-48,082,219Question Mark
Overlapping variant regions from other studies: 151 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):46,158,047-46,159,581Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5522286Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1748,080,68548,082,219
nsv5522286RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1746,158,04746,159,581

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713541deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713541Submitted genomicNC_000017.11:g.480
80685_48082219del
GRCh38 (hg38)NC_000017.11Chr1748,080,68548,082,219
nssv17713541RemappedPerfectNC_000017.10:g.461
58047_46159581del
GRCh37.p13First PassNC_000017.10Chr1746,158,04746,159,581

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)
nssv17713541<0.00116404
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