U.S. flag

An official website of the United States government

nsv6559281

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:794

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 25 studies. See in: genome view    
    Submitted genomic113,464,308-113,465,101Question Mark
    Overlapping variant regions from other studies: 135 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):113,183,155-113,183,948Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6559281Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3113,464,308113,465,101
    nsv6559281RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3113,183,155113,183,948

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18259232inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18259232Submitted genomicNC_000003.12:g.113
    464308_113465101in
    v
    GRCh38 (hg38)NC_000003.12Chr3113,464,308113,465,101
    nssv18259232RemappedPerfectNC_000003.11:g.113
    183155_113183948in
    v
    GRCh37.p13First PassNC_000003.11Chr3113,183,155113,183,948

    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)
    nssv18259232<0.001136972
    Support Center