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nsv6529577

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:680

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 343 SVs from 20 studies. See in: genome view    
    Submitted genomic76,132,620-76,133,299Question Mark
    Overlapping variant regions from other studies: 343 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):73,844,575-73,845,254Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6529577Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1876,132,62076,133,299
    nsv6529577RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1873,844,57573,845,254

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18044161deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18044161Submitted genomicNC_000018.10:g.761
    32620_76133299del
    GRCh38 (hg38)NC_000018.10Chr1876,132,62076,133,299
    nssv18044161RemappedPerfectNC_000018.9:g.7384
    4575_73845254del
    GRCh37.p13First PassNC_000018.9Chr1873,844,57573,845,254

    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)
    nssv18044161<0.001738304
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