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nsv6928998

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75,485

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 285 SVs from 47 studies. See in: genome view    
    Submitted genomic75,217,161-75,292,645Question Mark
    Overlapping variant regions from other studies: 285 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):75,610,941-75,686,425Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6928998Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1275,217,16175,292,645
    nsv6928998RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1275,610,94175,686,425

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18371973deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18371973Submitted genomicNC_000012.12:g.752
    17161_75292645del
    GRCh38 (hg38)NC_000012.12Chr1275,217,16175,292,645
    nssv18371973RemappedPerfectNC_000012.11:g.756
    10941_75686425del
    GRCh37.p13First PassNC_000012.11Chr1275,610,94175,686,425

    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)
    nssv183719734e-061274570
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