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nsv5449190

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 222 SVs from 46 studies. See in: genome view    
Submitted genomic131,351,000-131,408,000Question Mark
Overlapping variant regions from other studies: 222 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):131,069,844-131,126,844Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5449190Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3131,351,000131,408,000
nsv5449190RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3131,069,844131,126,844

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16937743duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16937743Submitted genomicNC_000003.12:g.131
351000_131408000du
p
GRCh38 (hg38)NC_000003.12Chr3131,351,000131,408,000
nssv16937743RemappedPerfectNC_000003.11:g.131
069844_131126844du
p
GRCh37.p13First PassNC_000003.11Chr3131,069,844131,126,844

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)
nssv16937743<0.00116404
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