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nsv6337450

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,976

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 252 SVs from 30 studies. See in: genome view    
    Submitted genomic174,738,747-174,769,722Question Mark
    Overlapping variant regions from other studies: 252 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):175,603,475-175,634,450Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6337450Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2174,738,747174,769,722
    nsv6337450RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2175,603,475175,634,450

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18207431duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18207431Submitted genomicNC_000002.12:g.174
    738747_174769722du
    p
    GRCh38 (hg38)NC_000002.12Chr2174,738,747174,769,722
    nssv18207431RemappedPerfectNC_000002.11:g.175
    603475_175634450du
    p
    GRCh37.p13First PassNC_000002.11Chr2175,603,475175,634,450

    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)
    nssv18207431<0.001139304
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