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nsv5397943

  • 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: 135 SVs from 29 studies. See in: genome view    
Submitted genomic120,706,628-120,706,679Question Mark
Overlapping variant regions from other studies: 135 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):120,425,475-120,425,526Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5397943Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3120,706,628120,706,679
nsv5397943RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3120,425,475120,425,526

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16938037alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16938037Submitted genomicNC_000003.12:g.120
706628_120706679in
s227
GRCh38 (hg38)NC_000003.12Chr3120,706,628120,706,679
nssv16938037RemappedPerfectNC_000003.11:g.120
425475_120425526in
s227
GRCh37.p13First PassNC_000003.11Chr3120,425,475120,425,526

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)
nssv169380370.1348606404
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