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nsv5443997

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:567

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
Submitted genomic179,138,847-179,139,413Question Mark
Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):178,856,635-178,857,201Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5443997Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3179,138,847179,139,413
nsv5443997RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3178,856,635178,857,201

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16943002duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16943002Submitted genomicNC_000003.12:g.179
138847_179139413du
p
GRCh38 (hg38)NC_000003.12Chr3179,138,847179,139,413
nssv16943002RemappedPerfectNC_000003.11:g.178
856635_178857201du
p
GRCh37.p13First PassNC_000003.11Chr3178,856,635178,857,201

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)
nssv16943002<0.00126404
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