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nsv6557948

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:354,240

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1356 SVs from 83 studies. See in: genome view    
    Submitted genomic125,753,835-126,108,074Question Mark
    Overlapping variant regions from other studies: 1356 SVs from 83 studies. See in: genome view    
    Remapped(Score: Perfect):125,393,889-125,748,128Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6557948Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7125,753,835126,108,074
    nsv6557948RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7125,393,889125,748,128

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18272985inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18272985Submitted genomicNC_000007.14:g.125
    753835_126108074in
    v
    GRCh38 (hg38)NC_000007.14Chr7125,753,835126,108,074
    nssv18272985RemappedPerfectNC_000007.13:g.125
    393889_125748128in
    v
    GRCh37.p13First PassNC_000007.13Chr7125,393,889125,748,128

    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)
    nssv18272985<0.001139304
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