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nsv6669066

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,847

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 156 SVs from 29 studies. See in: genome view    
    Submitted genomic62,202,826-62,221,672Question Mark
    Overlapping variant regions from other studies: 156 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):62,429,961-62,448,807Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6669066Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr262,202,82662,221,672
    nsv6669066RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr262,429,96162,448,807

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18467800deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18467800Submitted genomicNC_000002.12:g.622
    02826_62221672del
    GRCh38 (hg38)NC_000002.12Chr262,202,82662,221,672
    nssv18467800RemappedPerfectNC_000002.11:g.624
    29961_62448807del
    GRCh37.p13First PassNC_000002.11Chr262,429,96162,448,807

    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)
    nssv184678004e-061276256
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