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nsv5442118

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:79

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 110 SVs from 21 studies. See in: genome view    
Submitted genomic138,309,646-138,309,724Question Mark
Overlapping variant regions from other studies: 110 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):138,028,488-138,028,566Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5442118Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3138,309,646138,309,724
nsv5442118RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3138,028,488138,028,566

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16940010duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16940010Submitted genomicNC_000003.12:g.138
309646_138309724du
p
GRCh38 (hg38)NC_000003.12Chr3138,309,646138,309,724
nssv16940010RemappedPerfectNC_000003.11:g.138
028488_138028566du
p
GRCh37.p13First PassNC_000003.11Chr3138,028,488138,028,566

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)
nssv16940010<0.00116404
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