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nsv5449832

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:188

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 156 SVs from 25 studies. See in: genome view    
Submitted genomic138,832,806-138,832,993Question Mark
Overlapping variant regions from other studies: 156 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):138,551,648-138,551,835Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5449832Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3138,832,806138,832,993
nsv5449832RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3138,551,648138,551,835

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16940966deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16940966Submitted genomicNC_000003.12:g.138
832806_138832993de
l
GRCh38 (hg38)NC_000003.12Chr3138,832,806138,832,993
nssv16940966RemappedPerfectNC_000003.11:g.138
551648_138551835de
l
GRCh37.p13First PassNC_000003.11Chr3138,551,648138,551,835

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)
nssv16940966<0.00116404
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