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nsv5398422

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 22 studies. See in: genome view    
Submitted genomic138,272,419-138,272,470Question Mark
Overlapping variant regions from other studies: 108 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):137,991,261-137,991,312Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5398422Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3138,272,419138,272,470
nsv5398422RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3137,991,261137,991,312

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16940009alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16940009Submitted genomicNC_000003.12:g.138
272419_138272470in
s281
GRCh38 (hg38)NC_000003.12Chr3138,272,419138,272,470
nssv16940009RemappedPerfectNC_000003.11:g.137
991261_137991312in
s281
GRCh37.p13First PassNC_000003.11Chr3137,991,261137,991,312

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)
nssv169400090.003196404
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