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nsv6924541

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,646

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 163 SVs from 34 studies. See in: genome view    
    Submitted genomic64,270,214-64,285,859Question Mark
    Overlapping variant regions from other studies: 163 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):64,663,994-64,679,639Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6924541Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1264,270,21464,285,859
    nsv6924541RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1264,663,99464,679,639

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18371092deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18371092Submitted genomicNC_000012.12:g.642
    70214_64285859del
    GRCh38 (hg38)NC_000012.12Chr1264,270,21464,285,859
    nssv18371092RemappedPerfectNC_000012.11:g.646
    63994_64679639del
    GRCh37.p13First PassNC_000012.11Chr1264,663,99464,679,639

    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)
    nssv183710927e-062276264
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