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nsv4470824

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 48 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):193,240,915-193,240,915Question Mark
Overlapping variant regions from other studies: 48 SVs from 6 studies. See in: genome view    
Submitted genomic192,958,704-192,958,704Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4470824RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3193,240,915193,240,915
nsv4470824Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr3192,958,704192,958,704

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16052109alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16052109RemappedPerfectNC_000003.12:g.193
240915_193240916in
s281
GRCh38.p12First PassNC_000003.12Chr3193,240,915193,240,915
nssv16052109Submitted genomicNC_000003.11:g.192
958704_192958705in
s281
GRCh37.p13NC_000003.11Chr3192,958,704192,958,704

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)
nssv160521094.6e-005121692
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