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nsv5447873

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 59 SVs from 15 studies. See in: genome view    
Submitted genomic23,948,461-23,948,554Question Mark
Overlapping variant regions from other studies: 59 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):23,989,952-23,990,045Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5447873Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr323,948,46123,948,554
nsv5447873RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr323,989,95223,990,045

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16931080duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16931080Submitted genomicNC_000003.12:g.239
48461_23948554dup
GRCh38 (hg38)NC_000003.12Chr323,948,46123,948,554
nssv16931080RemappedPerfectNC_000003.11:g.239
89952_23990045dup
GRCh37.p13First PassNC_000003.11Chr323,989,95223,990,045

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)
nssv16931080<0.00126404
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