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nsv5453783

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,876

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 30 studies. See in: genome view    
Submitted genomic51,988,218-51,993,093Question Mark
Overlapping variant regions from other studies: 108 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):52,022,234-52,027,109Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5453783Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr351,988,21851,993,093
nsv5453783RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr352,022,23452,027,109

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16932738deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16932738Submitted genomicNC_000003.12:g.519
88218_51993093del
GRCh38 (hg38)NC_000003.12Chr351,988,21851,993,093
nssv16932738RemappedPerfectNC_000003.11:g.520
22234_52027109del
GRCh37.p13First PassNC_000003.11Chr352,022,23452,027,109

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)
nssv16932738<0.00116404
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