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nsv5474439

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:67

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 186 SVs from 20 studies. See in: genome view    
Submitted genomic103,407,386-103,407,452Question Mark
Overlapping variant regions from other studies: 186 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):104,419,614-104,419,680Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5474439Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8103,407,386103,407,452
nsv5474439RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8104,419,614104,419,680

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17014300duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17014300Submitted genomicNC_000008.11:g.103
407386_103407452du
p
GRCh38 (hg38)NC_000008.11Chr8103,407,386103,407,452
nssv17014300RemappedPerfectNC_000008.10:g.104
419614_104419680du
p
GRCh37.p13First PassNC_000008.10Chr8104,419,614104,419,680

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)
nssv17014300<0.00116404
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