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nsv4560202

  • 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: 28 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):119,484,918-119,484,918Question Mark
Overlapping variant regions from other studies: 28 SVs from 5 studies. See in: genome view    
Submitted genomic119,203,765-119,203,765Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4560202RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3119,484,918119,484,918
nsv4560202Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr3119,203,765119,203,765

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16048795sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16048795RemappedPerfectNC_000003.12:g.119
484918_119484919in
s1240
GRCh38.p12First PassNC_000003.12Chr3119,484,918119,484,918
nssv16048795Submitted genomicNC_000003.11:g.119
203765_119203766in
s1240
GRCh37.p13NC_000003.11Chr3119,203,765119,203,765

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)
nssv160487954.6e-005121694
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