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nsv6553345

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:568

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 167 SVs from 38 studies. See in: genome view    
    Submitted genomic129,970,888-129,971,455Question Mark
    Overlapping variant regions from other studies: 167 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):130,728,461-130,729,028Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6553345Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2129,970,888129,971,455
    nsv6553345RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2130,728,461130,729,028

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18256833inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18256833Submitted genomicNC_000002.12:g.129
    970888_129971455in
    v
    GRCh38 (hg38)NC_000002.12Chr2129,970,888129,971,455
    nssv18256833RemappedPerfectNC_000002.11:g.130
    728461_130729028in
    v
    GRCh37.p13First PassNC_000002.11Chr2130,728,461130,729,028

    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)
    nssv18256833<0.001235520
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