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nsv5439329

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:76,766

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 246 SVs from 49 studies. See in: genome view    
Submitted genomic40,356,416-40,433,181Question Mark
Overlapping variant regions from other studies: 246 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):40,397,907-40,474,672Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5439329Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr340,356,41640,433,181
nsv5439329RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr340,397,90740,474,672

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17730148deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17730148Submitted genomicNC_000003.12:g.403
56416_40433181del
GRCh38 (hg38)NC_000003.12Chr340,356,41640,433,181
nssv17730148RemappedPerfectNC_000003.11:g.403
97907_40474672del
GRCh37.p13First PassNC_000003.11Chr340,397,90740,474,672

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)
nssv17730148<0.00136404
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