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nsv6568042

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,877,559

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 22296 SVs from 122 studies. See in: genome view    
    Submitted genomic77,399,209-87,276,767Question Mark
    Overlapping variant regions from other studies: 22296 SVs from 122 studies. See in: genome view    
    Remapped(Score: Perfect):80,014,125-89,891,682Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6568042Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr977,399,20987,276,767
    nsv6568042RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr980,014,12589,891,682

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18281069inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18281069Submitted genomicNC_000009.12:g.773
    99209_87276767inv
    GRCh38 (hg38)NC_000009.12Chr977,399,20987,276,767
    nssv18281069RemappedPerfectNC_000009.11:g.800
    14125_89891682inv
    GRCh37.p13First PassNC_000009.11Chr980,014,12589,891,682

    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)
    nssv182810690.00518337116
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