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nsv5474318

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:58

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 273 SVs from 35 studies. See in: genome view    
Submitted genomic11,580,815-11,580,872Question Mark
Overlapping variant regions from other studies: 273 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):11,438,324-11,438,381Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5474318Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr811,580,81511,580,872
nsv5474318RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr811,438,32411,438,381

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17008302duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17008302Submitted genomicNC_000008.11:g.115
80815_11580872dup
GRCh38 (hg38)NC_000008.11Chr811,580,81511,580,872
nssv17008302RemappedPerfectNC_000008.10:g.114
38324_11438381dup
GRCh37.p13First PassNC_000008.10Chr811,438,32411,438,381

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)
nssv17008302<0.00116404
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