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nsv7073657

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,925,676

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 16822 SVs from 122 studies. See in: genome view    
    Submitted genomic3,848,628-8,774,303Question Mark
    Overlapping variant regions from other studies: 16828 SVs from 122 studies. See in: genome view    
    Remapped(Score: Perfect):3,751,922-8,677,621Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073657Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr173,848,6288,774,303
    nsv7073657RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr173,751,9228,677,621

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757254inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757254Submitted genomicNC_000017.11:g.384
    8628_8774303inv
    GRCh38 (hg38)NC_000017.11Chr173,848,6288,774,303
    nssv18757254RemappedPerfectNC_000017.10:g.375
    1922_8677621inv
    GRCh37.p13First PassNC_000017.10Chr173,751,9228,677,621

    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)
    nssv187572544e-061276268
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