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nsv5403762

  • 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: 111 SVs from 25 studies. See in: genome view    
Submitted genomic138,004,542-138,004,593Question Mark
Overlapping variant regions from other studies: 111 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):137,723,384-137,723,435Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5403762Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3138,004,542138,004,593
nsv5403762RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3137,723,384137,723,435

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16937858alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16937858Submitted genomicNC_000003.12:g.138
004542_138004593in
s281
GRCh38 (hg38)NC_000003.12Chr3138,004,542138,004,593
nssv16937858RemappedPerfectNC_000003.11:g.137
723384_137723435in
s281
GRCh37.p13First PassNC_000003.11Chr3137,723,384137,723,435

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)
nssv16937858<0.00116404
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