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nsv6584124

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,116,310

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3468 SVs from 122 studies. See in: genome view    
    Submitted genomic21,583,121-22,699,430Question Mark
    Overlapping variant regions from other studies: 3468 SVs from 122 studies. See in: genome view    
    Remapped(Score: Perfect):21,594,442-22,710,751Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6584124Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1621,583,12122,699,430
    nsv6584124RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1621,594,44222,710,751

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18239255inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18239255Submitted genomicNC_000016.10:g.215
    83121_22699430inv
    GRCh38 (hg38)NC_000016.10Chr1621,583,12122,699,430
    nssv18239255RemappedPerfectNC_000016.9:g.2159
    4442_22710751inv
    GRCh37.p13First PassNC_000016.9Chr1621,594,44222,710,751

    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)
    nssv182392550.4911877538238
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