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nsv6436928

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,138

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 21 studies. See in: genome view    
    Submitted genomic106,969,250-106,972,387Question Mark
    Overlapping variant regions from other studies: 104 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):108,729,008-108,732,145Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6436928Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10106,969,250106,972,387
    nsv6436928RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10108,729,008108,732,145

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17977608deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17977608Submitted genomicNC_000010.11:g.106
    969250_106972387de
    l
    GRCh38 (hg38)NC_000010.11Chr10106,969,250106,972,387
    nssv17977608RemappedPerfectNC_000010.10:g.108
    729008_108732145de
    l
    GRCh37.p13First PassNC_000010.10Chr10108,729,008108,732,145

    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)
    nssv17977608<0.001139144
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