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nsv5472347

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:709

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 104 SVs from 31 studies. See in: genome view    
Submitted genomic40,786,663-40,787,371Question Mark
Overlapping variant regions from other studies: 104 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):40,786,765-40,787,473Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5472347Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr540,786,66340,787,371
nsv5472347RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr540,786,76540,787,473

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16964496duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16964496Submitted genomicNC_000005.10:g.407
86663_40787371dup
GRCh38 (hg38)NC_000005.10Chr540,786,66340,787,371
nssv16964496RemappedPerfectNC_000005.9:g.4078
6765_40787473dup
GRCh37.p13First PassNC_000005.9Chr540,786,76540,787,473

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)
nssv16964496<0.00116404
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